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FDA 510(k)

UNIGRAFE

K-Number: K982699 · 1998-10-20

Decision Date1998-10-20
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNIGRAFE is the device name listed in this FDA 510(k) record. The listed applicant is Unicare Biomedical. It received FDA 510(k) clearance on 1998-10-20 under 510(k) number K982699. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIGRAFE?

UNIGRAFE is a medical device that received FDA 510(k) clearance on 1998-10-20. The listed applicant is Unicare Biomedical. The 510(k) number is K982699.

When did UNIGRAFE receive FDA 510(k) clearance?

UNIGRAFE received FDA 510(k) clearance on 1998-10-20, under 510(k) number K982699.

Who is the listed applicant for UNIGRAFE?

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

What is the FDA product code for UNIGRAFE?

The FDA product code for UNIGRAFE is LYC.

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 Unicare Biomedical 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: LYC)

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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