FDA 510(k)

PHYTACARE ALGINATE HYDROGEL WOUND DRESSING

K-Number: K980132 · 1998-06-26

Decision Date1998-06-26

Product CodeMGQ

DecisionSubstantially Equivalent for Some Indications

Device Summary

PHYTACARE ALGINATE HYDROGEL WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Phytatek Laboratories, Inc.. It received FDA 510(k) clearance on 1998-06-26 under 510(k) number K980132. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the PHYTACARE ALGINATE HYDROGEL WOUND DRESSING?

PHYTACARE ALGINATE HYDROGEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1998-06-26. The listed applicant is Phytatek Laboratories, Inc.. The 510(k) number is K980132.

When did PHYTACARE ALGINATE HYDROGEL WOUND DRESSING receive FDA 510(k) clearance?

PHYTACARE ALGINATE HYDROGEL WOUND DRESSING received FDA 510(k) clearance on 1998-06-26, under 510(k) number K980132.

Who is the listed applicant for PHYTACARE ALGINATE HYDROGEL WOUND DRESSING?

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

What is the FDA product code for PHYTACARE ALGINATE HYDROGEL WOUND DRESSING?

The FDA product code for PHYTACARE ALGINATE HYDROGEL WOUND DRESSING 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.