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FDA 510(k)

LEVTECH CLAMP APPLIER

K-Number: K874023 · 1987-11-06

ApplicantLevtech, Inc.
Decision Date1987-11-06
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LEVTECH CLAMP APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is Levtech, Inc.. It received FDA 510(k) clearance on 1987-11-06 under 510(k) number K874023. 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 LEVTECH CLAMP APPLIER?

LEVTECH CLAMP APPLIER is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Levtech, Inc.. The 510(k) number is K874023.

When did LEVTECH CLAMP APPLIER receive FDA 510(k) clearance?

LEVTECH CLAMP APPLIER received FDA 510(k) clearance on 1987-11-06, under 510(k) number K874023.

Who is the listed applicant for LEVTECH CLAMP APPLIER?

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

What is the FDA product code for LEVTECH CLAMP APPLIER?

The FDA product code for LEVTECH CLAMP APPLIER 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 Levtech, 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.

K910128LEVTECH TITANIUM BONE WIREK901144LEVTECH BONE SCREWK873693LEVTECH COMPOSITE TRACTION TONGSK850039HALIFAX SPINAL CLAMP

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.K974595CUSHING BAYONET, 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.

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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