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 dislodger, stone, flexible
510(k) Number K896322
Device Name CN GAURD, STERILE LATEX SURGICAL GLOVES
Applicant
C.N. TECHNOCRATS
108-13, 65TH RD.
FOREST HILLS,  NY  11375
Applicant Contact SANKAR NAIR
Correspondent
C.N. TECHNOCRATS
108-13, 65TH RD.
FOREST HILLS,  NY  11375
Correspondent Contact SANKAR NAIR
Regulation Number876.4680
Classification Product Code
FGO  
Date Received11/01/1989
Decision Date 07/12/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-