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FDA 510(k)

SURGICAL FORCEPS

K-Number: K890226 · 1989-01-27

ApplicantKinetic Medical Products
Decision Date1989-01-27
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Medical Products. It received FDA 510(k) clearance on 1989-01-27 under 510(k) number K890226. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL FORCEPS?

SURGICAL FORCEPS is a medical device that received FDA 510(k) clearance on 1989-01-27. The listed applicant is Kinetic Medical Products. The 510(k) number is K890226.

When did SURGICAL FORCEPS receive FDA 510(k) clearance?

SURGICAL FORCEPS received FDA 510(k) clearance on 1989-01-27, under 510(k) number K890226.

Who is the listed applicant for SURGICAL FORCEPS?

The FDA 510(k) record lists Kinetic Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL FORCEPS?

The FDA product code for SURGICAL FORCEPS is HTD.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Kinetic Medical Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K890385MIDWIFERY/OBSTETRICAL FORCEPSK890387MALLEABLE PLACENTA CURETTEK890380CERVICAL BIOPSY FORCEPSK890376VAGINAL SPECULUMK890382COMPRESSION FORCEPSK890383HYSTERECTOMY FORCEPS

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Related Devices (Code: HTD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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