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FDA 510(k)

HYCOAT

K-Number: K960686 · 1996-08-12

ApplicantThe Hymed Group Corp.
Decision Date1996-08-12
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

HYCOAT 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 1996-08-12 under 510(k) number K960686. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the HYCOAT?

HYCOAT is a medical device that received FDA 510(k) clearance on 1996-08-12. The listed applicant is The Hymed Group Corp.. The 510(k) number is K960686.

When did HYCOAT receive FDA 510(k) clearance?

HYCOAT received FDA 510(k) clearance on 1996-08-12, under 510(k) number K960686.

Who is the listed applicant for HYCOAT?

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 HYCOAT?

The FDA product code for HYCOAT is MGQ.

Related Clinical Trials

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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 GELK961930CHONDROPROTECK955506HYCURE

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

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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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