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 Needle, Hypodermic, Single Lumen
510(k) Number K901162
Device Name STERIMATIC(TM) SAFETY NEEDLE
Applicant
Sterimatic Worldwide, Ltd.
Abnash, Chalford Hill
Stroud, Gloucestershire,  GB GL6 8QN
Applicant Contact JOHN S PARRY
Correspondent
Sterimatic Worldwide, Ltd.
Abnash, Chalford Hill
Stroud, Gloucestershire,  GB GL6 8QN
Correspondent Contact JOHN S PARRY
Regulation Number880.5570
Classification Product Code
FMI  
Date Received03/13/1990
Decision Date 09/28/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-