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, Obstetrical
510(k) Number K905583
Device Name ILC FORCEPS PADS
Applicant
Inman Liebelt Corp.
P.O. Box 171077
Arlington,  TX  76003
Applicant Contact ROGER LIEBELT
Correspondent
Inman Liebelt Corp.
P.O. Box 171077
Arlington,  TX  76003
Correspondent Contact ROGER LIEBELT
Regulation Number884.4400
Classification Product Code
HDA  
Date Received12/12/1990
Decision Date 04/12/1991
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
-
-