• 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 K851106
Device Name PRATT-SMITH T FORCEPS 1830-40 PCS. SS 420 OR 420F
Applicant
THE HUXLEY INSTRUMENT CORP.
215 MAIN ST.
PENN YAN,  NY  14527
Applicant Contact REBECCA J SHAHZADA
Correspondent
THE HUXLEY INSTRUMENT CORP.
215 MAIN ST.
PENN YAN,  NY  14527
Correspondent Contact REBECCA J SHAHZADA
Regulation Number878.4800
Classification Product Code
GEN  
Date Received03/19/1985
Decision Date 04/25/1985
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
-
-