FDA 510(k)

IAMIN GEL WOUND DRESSING

K-Number: K953853 · 1996-02-05

Decision Date1996-02-05

Product CodeMGQ

DecisionSubstantially Equivalent for Some Indications

Device Summary

IAMIN GEL WOUND 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 1996-02-05 under 510(k) number K953853. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the IAMIN GEL WOUND DRESSING?

IAMIN GEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1996-02-05. The listed applicant is Procyte Corp.. The 510(k) number is K953853.

When did IAMIN GEL WOUND DRESSING receive FDA 510(k) clearance?

IAMIN GEL WOUND DRESSING received FDA 510(k) clearance on 1996-02-05, under 510(k) number K953853.

Who is the listed applicant for IAMIN GEL WOUND 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 GEL WOUND DRESSING?

The FDA product code for IAMIN GEL WOUND DRESSING is MGQ.

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Other records listing Procyte Corp. as applicant

K971612OSMO/PCA PILLOW WOUND DRESSING K972329OSMOCYTE RA WOUND DRESSING K972150OSMOCYTE ISLAND WOUND DRESSING K970153LAMIN-2 HYDRATING GEL K965143OSMOCYTE WOUND MANAGER SHEET DRESSING K965005IAMIN IMPREGNATED GAUZE DRESSING

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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.