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FDA 510(k)

TECNOL QUICK RELEASE LIMB HOLDER

K-Number: K801272 · 1980-06-17

Decision Date1980-06-17
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TECNOL QUICK RELEASE LIMB HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Tecnol New Jersey Wound Care, Inc.. It received FDA 510(k) clearance on 1980-06-17 under 510(k) number K801272. The device is classified under product code FMQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECNOL QUICK RELEASE LIMB HOLDER?

TECNOL QUICK RELEASE LIMB HOLDER is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Tecnol New Jersey Wound Care, Inc.. The 510(k) number is K801272.

When did TECNOL QUICK RELEASE LIMB HOLDER receive FDA 510(k) clearance?

TECNOL QUICK RELEASE LIMB HOLDER received FDA 510(k) clearance on 1980-06-17, under 510(k) number K801272.

Who is the listed applicant for TECNOL QUICK RELEASE LIMB HOLDER?

The FDA 510(k) record lists Tecnol New Jersey Wound Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TECNOL QUICK RELEASE LIMB HOLDER?

The FDA product code for TECNOL QUICK RELEASE LIMB HOLDER is FMQ.

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.

Other records listing Tecnol New Jersey Wound Care, 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.

View all 35 devices →

Related Devices (Code: FMQ)

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.

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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