• 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 Gauze/Sponge, Internal
510(k) Number K872808
Device Name CHEVRON TAPE DISSECTOR, 9/16 X 1/4, 9/16 X 1/8
Applicant
American Silk Sutures, Inc.
57 Munroe St.
Lynn,  MA  01901
Applicant Contact ED GREENSPAN
Correspondent
American Silk Sutures, Inc.
57 Munroe St.
Lynn,  MA  01901
Correspondent Contact ED GREENSPAN
Classification Product Code
EFQ  
Date Received07/14/1987
Decision Date 08/04/1987
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-