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 blade, scalpel
510(k) Number K851157
Device Name SURGIMED - SURGICAL BLADES
Applicant
SURGIMED CORP.
ONE OAK BORRK TERRANCE #500
22ND. AT BUTTERFIELD ROAD
OAKBROOK TERRANCE,  IL  60181
Applicant Contact PARVEZ SHIRZAI
Correspondent
SURGIMED CORP.
ONE OAK BORRK TERRANCE #500
22ND. AT BUTTERFIELD ROAD
OAKBROOK TERRANCE,  IL  60181
Correspondent Contact PARVEZ SHIRZAI
Regulation Number878.4800
Classification Product Code
GES  
Date Received03/22/1985
Decision Date 04/25/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-