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FDA 510(k)

IAMIN IMPREGNATED GAUZE DRESSING

K-Number: K965005 · 1997-02-24

ApplicantProcyte Corp.
Decision Date1997-02-24
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

IAMIN IMPREGNATED GAUZE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Procyte Corp.. It received FDA 510(k) clearance on 1997-02-24 under 510(k) number K965005. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IAMIN IMPREGNATED GAUZE DRESSING?

IAMIN IMPREGNATED GAUZE DRESSING is a medical device that received FDA 510(k) clearance on 1997-02-24. The listed applicant is Procyte Corp.. The 510(k) number is K965005.

When did IAMIN IMPREGNATED GAUZE DRESSING receive FDA 510(k) clearance?

IAMIN IMPREGNATED GAUZE DRESSING received FDA 510(k) clearance on 1997-02-24, under 510(k) number K965005.

Who is the listed applicant for IAMIN IMPREGNATED GAUZE DRESSING?

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

What is the FDA product code for IAMIN IMPREGNATED GAUZE DRESSING?

The FDA product code for IAMIN IMPREGNATED GAUZE DRESSING is MGQ.

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Other records listing Procyte 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.

K971612OSMO/PCA PILLOW WOUND DRESSINGK972150OSMOCYTE ISLAND WOUND DRESSINGK972329OSMOCYTE RA WOUND DRESSINGK970153LAMIN-2 HYDRATING GELK965143OSMOCYTE WOUND MANAGER SHEET DRESSINGK964468IAMIN WET DRESSING (COPPER-SALINE)

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Related Devices (Code: MGQ)

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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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