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510(k) K905583

Device
ILC FORCEPS PADS
Applicant
INMAN LIEBELT CORP.
510(k) number
K905583
Product code
HDA  
Decision
Substantially Equivalent (SESE)
Decision date
1991-04-12
Date received
1990-12-12
Regulation
884.4400
Classification name
Forceps, Obstetrical
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
ROGER LIEBELT
Address
P.O. Box 171077 Arlington TX US 76003 76003

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HDA  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K100517INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXXInstrumed International, Inc.2010-04-29
K092827DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XXDimeda Instrumente GmbH2010-01-08
K013747TEKNO-MEDICAL OBSTETRICAL FORCEPSTekno Medical Optik-Chirurgie GmbH & Co.2002-02-11
K951529V. MUELLER OBSTETRICAL (OB) FORCEPSBaxter Healthcare Corp1995-08-04
K914552CMI VACUUM PUMPColumbia Medical & Surgical, Inc.1993-09-07
K903205AUTO SUTURE(R) ENDOSCOPIC CLAMPUnited States Surgical, A Division of Tyco Healthc1990-10-11
K890385MIDWIFERY/OBSTETRICAL FORCEPSKinetic Medical Products1989-03-01
K851883SIMPSON OBSTETRICAL FORCEPS-SS TYPE 410 OR 420The Huxley Instrument Corp.1985-05-09
K771106FORCEPS, OB, NON-COMPRESSIVEZeppelin Medizinlechnik GmbH1977-07-01

Legacy Summary#

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FDA Review#

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