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Recognition List Number: 028 Publication Date: 03/16/2012 

Part B: SUPPLEMENTARY INFORMATION

Recognition Number 14-274: AAMI / ANSI / ISO 15882:2008, Sterilization of health care products - Chemical indicators - Guidance for selection, use, and interpretation of results. (Sterility)

Date of Standard: 2008. 
Addresses of Standards Organizations:
  Association for the Advancement of Medical Instrumentation (AAMI)
  4301 North Fairfax Drive
  Suite 301
  Arlington, VA 22203
 
  American National Standards Institute (ANSI)
  25 West 43rd Street
  4th Floor
  New York, NY 10036
 
  International Organization for Standardization (ISO)*
  1, Rue de Varembe
  Case Postale 56
  CH 1211 Geneva 20, 0
  SWITZERLAND
CDRH Offices and Divisions Associated with Recognized Standards:
(1)OFFICE OF DEVICE EVALUATION (ODE)
(2)OFFICE OF COMPLIANCE (OC)
Devices Affected:
Chemical indicators intended for use by health care facilities
Processes Affected:
510(k), PMA, PDP, IDE, HDE, Design Control Input, Quality System Regulation
Type of Standard:
 Vertical
Extent of Recognition:
(Note: Three types of chemical indicators are cleared by the FDA - Process indicators, Chemical integrators and Air removal indicators for test pack. Unlike the ISO chemical indicator classes, FDA does not use numerical classes to designate chemical indicators. Performance characteristics specified for the following ISO Chemical Indicator classes are recognized by FDA.)

Recognized for Class 1: Process indicators Section 4.2

Recognized for Class 2: Indicators for use in specific tests Section 4.3

Recognized for Class 6: Emulating indicators Section 4.7; performance characteristics should be demonstrated to be equivalent to a legally marketed predicate device

In addition, provide the following data:

1. Resistometer testing for chemical indicators.

2. Emulating indicators (Class 6):

a. Side-by-side (same chamber) testing of emulating indicators with appropriate biological indicators (BIs). FDA recommends that the resistance characteristics of the BIs be consistent with minimum performance characteristics described in the guidance "Guidance for Industry and FDA Staff: Biological indicator (BI) Premarket Notification [510(k)] Submissions. October 4, 2007"

b. Characterization of performance by varying only one parameter at a time.

3. Testing in an actual sterilizer used in health care facility.

4. Shelf life testing and stability testing of end-point color reaction for all chemical indicators.

5. Data showing that the endpoint specifications for all chemical indicators correlate with standard sterilization cycles used in health care facilities.
Related CFR Citations and Product Codes:
Regulation
Number
Device Name Device
Class
Product
Code
§880.2800 Indicator, Physical/Chemical Sterilization Process Class 2 JOJ
§880.2800 Indicator, Sterilization Class 2 LRT
§880.2800 Indicator,Chemical,Enzymatic,Sterilization Process Class 2 MTC
 
Relevant Guidance:
"Premarket Notification [510(k)] Submissions for Chemical Indicators: Guidance for Industry and FDA Staff, December 19, 2003"

"Premarket Notifications [510(k)] for Biological Indicators Intended to Monitor Sterilizers Used in Health Care Facilities: Draft Guide for Industry and FDA Reviewers, May 21, 2001
FDA Technical Contact:
  Geetha C. Jayan, M.V.Sc, Ph.D
  FDA/CDRH/OCD
  10903 New Hampshire Avenue Building 66, Room 5400
  Silver Spring MD 20993
  301/796-6300
  Email: geetha.jayan@fda.hhs.gov
* In the United States, copies of this standard can be obtained from:
  American National Standards Institute (ANSI)*
  25 West 43rd Street
  4th Floor
  New York, NY 10036
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