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FDA 510(k)

BIAFINE

K-Number: K943910 · 1995-02-27

ApplicantLaboratoire Medix
Decision Date1995-02-27
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

BIAFINE is the device name listed in this FDA 510(k) record. The listed applicant is Laboratoire Medix. It received FDA 510(k) clearance on 1995-02-27 under 510(k) number K943910. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIAFINE?

BIAFINE is a medical device that received FDA 510(k) clearance on 1995-02-27. The listed applicant is Laboratoire Medix. The 510(k) number is K943910.

When did BIAFINE receive FDA 510(k) clearance?

BIAFINE received FDA 510(k) clearance on 1995-02-27, under 510(k) number K943910.

Who is the listed applicant for BIAFINE?

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

What is the FDA product code for BIAFINE?

The FDA product code for BIAFINE is MGQ.

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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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