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FDA 510(k)

CUSHING BAYONET, INSULATED BIPOLAR FORCEP

K-Number: K974595 · 1998-06-24

ApplicantTitan Mfg., Inc.
Decision Date1998-06-24
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CUSHING BAYONET, INSULATED BIPOLAR FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is Titan Mfg., Inc.. It received FDA 510(k) clearance on 1998-06-24 under 510(k) number K974595. 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 CUSHING BAYONET, INSULATED BIPOLAR FORCEP?

CUSHING BAYONET, INSULATED BIPOLAR FORCEP is a medical device that received FDA 510(k) clearance on 1998-06-24. The listed applicant is Titan Mfg., Inc.. The 510(k) number is K974595.

When did CUSHING BAYONET, INSULATED BIPOLAR FORCEP receive FDA 510(k) clearance?

CUSHING BAYONET, INSULATED BIPOLAR FORCEP received FDA 510(k) clearance on 1998-06-24, under 510(k) number K974595.

Who is the listed applicant for CUSHING BAYONET, INSULATED BIPOLAR FORCEP?

The FDA 510(k) record lists Titan Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUSHING BAYONET, INSULATED BIPOLAR FORCEP?

The FDA product code for CUSHING BAYONET, INSULATED BIPOLAR FORCEP is HTD.

Related Clinical Trials

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 Titan Mfg., Inc. 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.

K974594SEMKIN BIPOLAR FORCEPK974593SEMKIN INSULATED BIPOLAR FORCEP

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.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, Inc.K895212TIK EXTRAKTORInstruments of Sweden, 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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