TECNOL HYDROGEL WOUND DRESSING
K-Number: K955575 · 1996-01-17
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Device Summary
Frequently Asked Questions
What is the TECNOL HYDROGEL WOUND DRESSING?
TECNOL HYDROGEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1996-01-17. The listed applicant is Tecnol Medical Products, Inc.. The 510(k) number is K955575.
When did TECNOL HYDROGEL WOUND DRESSING receive FDA 510(k) clearance?
TECNOL HYDROGEL WOUND DRESSING received FDA 510(k) clearance on 1996-01-17, under 510(k) number K955575.
Who is the listed applicant for TECNOL HYDROGEL WOUND DRESSING?
The FDA 510(k) record lists Tecnol Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TECNOL HYDROGEL WOUND DRESSING?
The FDA product code for TECNOL 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 Tecnol Medical Products, 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.
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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