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 Instrument, Surgical, Disposable
510(k) Number K912834
Device Name SHUR-GRIP
Applicant
Inman Medical Corp.
P.O. Box 171077
Arlington,  TX  76003
Applicant Contact CLAY WILSON
Correspondent
Inman Medical Corp.
P.O. Box 171077
Arlington,  TX  76003
Correspondent Contact CLAY WILSON
Regulation Number878.4800
Classification Product Code
KDC  
Date Received06/26/1991
Decision Date 07/26/1991
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
Predetermined Change
Control Plan Authorized		 No
-
-