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, Biopsy, Gynecological
510(k) Number K926538
Device Name TISCHLER BIOPSY FORCEPS
Applicant
Thomasville Medical Assoc.
935 Cobblestone Court
Alpharetta,  GA  30201
Applicant Contact THOMAS J ZINNANTI
Correspondent
Thomasville Medical Assoc.
935 Cobblestone Court
Alpharetta,  GA  30201
Correspondent Contact THOMAS J ZINNANTI
Regulation Number884.4530
Classification Product Code
HFB  
Date Received12/30/1992
Decision Date 02/24/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-