Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Antisera, Fluorescent, All Types, Streptococcus Pneumoniae
510(k) Number K760816
Device Name PNEUMOTACHOGRAPHY SYSTEM
Applicant
Aftercal, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Aftercal, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.3740
Classification Product Code
GWB  
Date Received10/12/1976
Decision Date 10/29/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-