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FDA 510(k)

C-GRAFT

K-Number: K033110 · 2003-12-10

ApplicantThe Clinician'S Preference, LLC
Decision Date2003-12-10
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

C-GRAFT is the device name listed in this FDA 510(k) record. The listed applicant is The Clinician'S Preference, LLC. It received FDA 510(k) clearance on 2003-12-10 under 510(k) number K033110. 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 C-GRAFT?

C-GRAFT is a medical device that received FDA 510(k) clearance on 2003-12-10. The listed applicant is The Clinician'S Preference, LLC. The 510(k) number is K033110.

When did C-GRAFT receive FDA 510(k) clearance?

C-GRAFT received FDA 510(k) clearance on 2003-12-10, under 510(k) number K033110.

Who is the listed applicant for C-GRAFT?

The FDA 510(k) record lists The Clinician'S Preference, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C-GRAFT?

The FDA product code for C-GRAFT is LYC.

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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.

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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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