PATIENT PROTECTIVE LIMB
K-Number: K962626 · 1996-10-02
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Device Summary
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
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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