SINCLAIR WOUND AND SKIN EMULSION
K-Number: K024367 · 2003-07-28
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Device Summary
Frequently Asked Questions
What is the SINCLAIR WOUND AND SKIN EMULSION?
SINCLAIR WOUND AND SKIN EMULSION is a medical device that received FDA 510(k) clearance on 2003-07-28. The listed applicant is Sinclair Pharmaceuticals, Ltd.. The 510(k) number is K024367.
When did SINCLAIR WOUND AND SKIN EMULSION receive FDA 510(k) clearance?
SINCLAIR WOUND AND SKIN EMULSION received FDA 510(k) clearance on 2003-07-28, under 510(k) number K024367.
Who is the listed applicant for SINCLAIR WOUND AND SKIN EMULSION?
The FDA 510(k) record lists Sinclair Pharmaceuticals, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SINCLAIR WOUND AND SKIN EMULSION?
The FDA product code for SINCLAIR WOUND AND SKIN EMULSION 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 Sinclair Pharmaceuticals, 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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