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FDA 510(k)

GLUCANPRO CREAM

K-Number: K002077 · 2000-10-02

ApplicantBrennen Medical, Inc.
Decision Date2000-10-02
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

GLUCANPRO CREAM is the device name listed in this FDA 510(k) record. The listed applicant is Brennen Medical, Inc.. It received FDA 510(k) clearance on 2000-10-02 under 510(k) number K002077. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLUCANPRO CREAM?

GLUCANPRO CREAM is a medical device that received FDA 510(k) clearance on 2000-10-02. The listed applicant is Brennen Medical, Inc.. The 510(k) number is K002077.

When did GLUCANPRO CREAM receive FDA 510(k) clearance?

GLUCANPRO CREAM received FDA 510(k) clearance on 2000-10-02, under 510(k) number K002077.

Who is the listed applicant for GLUCANPRO CREAM?

The FDA 510(k) record lists Brennen Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLUCANPRO CREAM?

The FDA product code for GLUCANPRO CREAM is MGQ.

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Other records listing Brennen Medical, Inc. 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.

K050086BRENNEN MEDICAL SILVER GLUCAN WOUND DRESSINGK030460MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIXK021835BRENNEN MEDICAL SURGICAL MESH, GLUCAMESH/GLUCATEXK002078BETA GLUCAN GEL (MACROPRO GEL)K000519GLUCANPROK000518MACROPRO GEL

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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.

K171879HylaGuard Moisturizing CreamFounders Science Group, LLCK083024HYLATOPIC EMOLLIENT FOAMCollegium Pharmaceutical IncorporatedK041342IMPRUV A.I. CREAM WOUND AND SKIN EMULSIONStiefel Laboratories, Inc.K041268SILVERSITE OR CALGITROLAdriK040019SILVERSEALNoble Fiber TechnologiesK040517TENDERWET ACTIVEMedline Industries, Inc.

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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