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510(k) K890238

Device
CATHETER FORCEPS
Applicant
KINETIC MEDICAL PRODUCTS
510(k) number
K890238
Product code
HTD  
Decision
Substantially Equivalent (SESE)
Decision date
1989-01-27
Date received
1989-01-18
Regulation
878.4800
Classification name
Forceps
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
JAMES I LAUGHNER
Address
4934 Peach St. Erie PA US 16509 16509

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HTD  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K051281THE NEEDLE CATCHERE.D.Medical , Ltd.2005-09-08
K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.1998-06-24
K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.1998-06-24
K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.1998-06-24
K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical Technology1991-10-23
K911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, Inc.1991-03-29
K895212TIK EXTRAKTORInstruments of Sweden, Inc.1989-09-27
K890373HEMORRHOIDAL FORCEPSKinetic Medical Products1989-02-03
K890369GALL STONE FORCEPSKinetic Medical Products1989-02-03
K890257BONE CUTTING FORCEPS, DOUBLE-ACTIONKinetic Medical Products1989-01-27
K890263CILIA FORCEPSKinetic Medical Products1989-01-27
K890262LUNG FORCEPSKinetic Medical Products1989-01-27
K890260BONE SHEARSKinetic Medical Products1989-01-27
K890259RIB SHEARSKinetic Medical Products1989-01-27
K890258BONE CUTTING FORCEPS, SINGLE-ACTIONKinetic Medical Products1989-01-27

Legacy Summary#

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FDA Review#

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