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 forceps, general & plastic surgery
510(k) Number K884514
Device Name FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL
Applicant
GATEWOOD AND ASSOCIATES, LTD.
P.O. BOX 324
TACOMA,  WA  98401
Applicant Contact ELTON GATEWOOD
Correspondent
GATEWOOD AND ASSOCIATES, LTD.
P.O. BOX 324
TACOMA,  WA  98401
Correspondent Contact ELTON GATEWOOD
Regulation Number878.4800
Classification Product Code
GEN  
Date Received10/27/1988
Decision Date 11/17/1988
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
-
-