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 Surgeon'S Gloves
510(k) Number K892495
Device Name SURGEON'S GLOVES
Applicant
Care-Pro Industries, Inc.
10605 Boomer Cir.
Suite 101
Dallas,  TX  75238
Applicant Contact ALEX LAI
Correspondent
Care-Pro Industries, Inc.
10605 Boomer Cir.
Suite 101
Dallas,  TX  75238
Correspondent Contact ALEX LAI
Regulation Number878.4460
Classification Product Code
KGO  
Date Received04/13/1989
Decision Date 10/11/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-