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 Gauze/Sponge, Internal, X-Ray Detectable
510(k) Number K780718
Device Name SOF-WICKLAP PAD
Applicant
Johnson & Johnson Professionals, Inc.
501 George St.
New Brunswick,  NJ  08903
Applicant Contact Jean Grieve
Correspondent
Johnson & Johnson Professionals, Inc.
501 George St.
New Brunswick,  NJ  08903
Correspondent Contact Jean Grieve
Regulation Number878.4450
Classification Product Code
GDY  
Date Received05/01/1978
Decision Date 06/28/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-