CARASYN HYDROGEL WOUND PRODUCTS
K-Number: K961758 · 1996-07-11
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Device Summary
Frequently Asked Questions
What is the CARASYN HYDROGEL WOUND PRODUCTS?
CARASYN HYDROGEL WOUND PRODUCTS is a medical device that received FDA 510(k) clearance on 1996-07-11. The listed applicant is Carrington Laboratories, Inc.. The 510(k) number is K961758.
When did CARASYN HYDROGEL WOUND PRODUCTS receive FDA 510(k) clearance?
CARASYN HYDROGEL WOUND PRODUCTS received FDA 510(k) clearance on 1996-07-11, under 510(k) number K961758.
Who is the listed applicant for CARASYN HYDROGEL WOUND PRODUCTS?
The FDA 510(k) record lists Carrington Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARASYN HYDROGEL WOUND PRODUCTS?
The FDA product code for CARASYN HYDROGEL WOUND PRODUCTS 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 Carrington Laboratories, 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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