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FDA 510(k)

CHONDROPROTEC

K-Number: K961930 · 1996-10-15

ApplicantThe Hymed Group Corp.
Decision Date1996-10-15
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

CHONDROPROTEC is the device name listed in this FDA 510(k) record. The listed applicant is The Hymed Group Corp.. It received FDA 510(k) clearance on 1996-10-15 under 510(k) number K961930. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the CHONDROPROTEC?

CHONDROPROTEC is a medical device that received FDA 510(k) clearance on 1996-10-15. The listed applicant is The Hymed Group Corp.. The 510(k) number is K961930.

When did CHONDROPROTEC receive FDA 510(k) clearance?

CHONDROPROTEC received FDA 510(k) clearance on 1996-10-15, under 510(k) number K961930.

Who is the listed applicant for CHONDROPROTEC?

The FDA 510(k) record lists The Hymed Group Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHONDROPROTEC?

The FDA product code for CHONDROPROTEC is MGQ.

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 The Hymed Group Corp. 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.

K061227HYDROLYZED COLLAGEN/AG WOUND GEL WITH SILVERK994339HYCURE ORAL / HYCURE ORAL SMART GELK960686HYCOATK955506HYCURE

Related Devices (Code: MGQ)

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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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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