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 Bronchoscope (Flexible Or Rigid)
510(k) Number K926430
Device Name CANNULATED BIOPSY FORCEPS
Applicant
Thomasville Medical Assoc.
935 Cobblestone Ct.
Alpharetta,  GA  30201
Applicant Contact THOMAS J ZINNANTI
Correspondent
Thomasville Medical Assoc.
935 Cobblestone Ct.
Alpharetta,  GA  30201
Correspondent Contact THOMAS J ZINNANTI
Regulation Number874.4680
Classification Product Code
EOQ  
Date Received12/23/1992
Decision Date 03/26/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-