SILVAKLENZ SKIN AND WOUND CLENSER SOLUTION
K-Number: K063069 · 2007-07-13
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Device Summary
Frequently Asked Questions
What is the SILVAKLENZ SKIN AND WOUND CLENSER SOLUTION?
SILVAKLENZ SKIN AND WOUND CLENSER SOLUTION is a medical device that received FDA 510(k) clearance on 2007-07-13. The listed applicant is Medical Molecular Therapuetics, LLC. The 510(k) number is K063069.
When did SILVAKLENZ SKIN AND WOUND CLENSER SOLUTION receive FDA 510(k) clearance?
SILVAKLENZ SKIN AND WOUND CLENSER SOLUTION received FDA 510(k) clearance on 2007-07-13, under 510(k) number K063069.
Who is the listed applicant for SILVAKLENZ SKIN AND WOUND CLENSER SOLUTION?
The FDA 510(k) record lists Medical Molecular Therapuetics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SILVAKLENZ SKIN AND WOUND CLENSER SOLUTION?
The FDA product code for SILVAKLENZ SKIN AND WOUND CLENSER SOLUTION is FRO. This falls under the Anesthesiology category.
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 Medical Molecular Therapuetics, LLC 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: FRO)
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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