M-K HYDROGEL DRESSING
K-Number: K940409 · 1994-07-11
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Device Summary
Frequently Asked Questions
What is the M-K HYDROGEL DRESSING?
M-K HYDROGEL DRESSING is a medical device that received FDA 510(k) clearance on 1994-07-11. The listed applicant is Mason-Keller Corp.. The 510(k) number is K940409.
When did M-K HYDROGEL DRESSING receive FDA 510(k) clearance?
M-K HYDROGEL DRESSING received FDA 510(k) clearance on 1994-07-11, under 510(k) number K940409.
Who is the listed applicant for M-K HYDROGEL DRESSING?
The FDA 510(k) record lists Mason-Keller Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for M-K HYDROGEL DRESSING?
The FDA product code for M-K HYDROGEL 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 Mason-Keller 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.
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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