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FDA 510(k)

PATIENT PROTECTIVE LIMB

K-Number: K962626 · 1996-10-02

Decision Date1996-10-02
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT PROTECTIVE LIMB is the device name listed in this FDA 510(k) record. The listed applicant is Kenad SG Medical, Inc.. It received FDA 510(k) clearance on 1996-10-02 under 510(k) number K962626. 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 PATIENT PROTECTIVE LIMB?

PATIENT PROTECTIVE LIMB is a medical device that received FDA 510(k) clearance on 1996-10-02. The listed applicant is Kenad SG Medical, Inc.. The 510(k) number is K962626.

When did PATIENT PROTECTIVE LIMB receive FDA 510(k) clearance?

PATIENT PROTECTIVE LIMB received FDA 510(k) clearance on 1996-10-02, under 510(k) number K962626.

Who is the listed applicant for PATIENT PROTECTIVE LIMB?

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

What is the FDA product code for PATIENT PROTECTIVE LIMB?

The FDA product code for PATIENT PROTECTIVE LIMB 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 Kenad SG Medical, 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.

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

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

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