FLEXIGEL-G HYDROGEL WOUND DRESSING
K-Number: K980097 · 1998-03-04
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Device Summary
Frequently Asked Questions
What is the FLEXIGEL-G HYDROGEL WOUND DRESSING?
FLEXIGEL-G HYDROGEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1998-03-04. The listed applicant is Innovative Technologies , Ltd.. The 510(k) number is K980097.
When did FLEXIGEL-G HYDROGEL WOUND DRESSING receive FDA 510(k) clearance?
FLEXIGEL-G HYDROGEL WOUND DRESSING received FDA 510(k) clearance on 1998-03-04, under 510(k) number K980097.
Who is the listed applicant for FLEXIGEL-G HYDROGEL WOUND DRESSING?
The FDA 510(k) record lists Innovative Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIGEL-G HYDROGEL WOUND DRESSING?
The FDA product code for FLEXIGEL-G HYDROGEL WOUND DRESSING is MGQ.
Related Clinical Trials
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.
Other records listing Innovative Technologies , Ltd. 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.
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.
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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