• 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, surgical, gynecological
510(k) Number K901897
Device Name ZEPPELIN FORCEPS
Applicant
KIRWAN SURGICAL PRODUCTS, INC.
83 E. WATER ST.
P.O. BOX 545
ROCKLAND,  MA  02370
Applicant Contact KIRWAN, JR.
Correspondent
KIRWAN SURGICAL PRODUCTS, INC.
83 E. WATER ST.
P.O. BOX 545
ROCKLAND,  MA  02370
Correspondent Contact KIRWAN, JR.
Regulation Number884.4530
Classification Product Code
HCZ  
Date Received04/25/1990
Decision Date 06/29/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-