HYDRO-M(TM) WOUND GEL
K-Number: K940814 · 1994-05-12
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Device Summary
Frequently Asked Questions
What is the HYDRO-M(TM) WOUND GEL?
HYDRO-M(TM) WOUND GEL is a medical device that received FDA 510(k) clearance on 1994-05-12. The listed applicant is Kingston Technologies, Inc.. The 510(k) number is K940814.
When did HYDRO-M(TM) WOUND GEL receive FDA 510(k) clearance?
HYDRO-M(TM) WOUND GEL received FDA 510(k) clearance on 1994-05-12, under 510(k) number K940814.
Who is the listed applicant for HYDRO-M(TM) WOUND GEL?
The FDA 510(k) record lists Kingston Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HYDRO-M(TM) WOUND GEL?
The FDA product code for HYDRO-M(TM) WOUND GEL 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 Kingston Technologies, 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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