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 Gown, Surgical
510(k) Number K041540
Device Name COMBOSAFE (EUROPE) AND PROMAX (US) SURGICAL GOWNS
Applicant
Standard Textile Co., Inc.
One Knollcrest Dr.
Cincinnati,  OH  45237 -1600
Applicant Contact BRADLEY J BUSHMAN
Correspondent
Standard Textile Co., Inc.
One Knollcrest Dr.
Cincinnati,  OH  45237 -1600
Correspondent Contact BRADLEY J BUSHMAN
Regulation Number878.4040
Classification Product Code
FYA  
Date Received06/08/2004
Decision Date 05/05/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-