DIMISIL SCAR GEL
K-Number: K023678 · 2003-01-23
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Device Summary
Frequently Asked Questions
What is the DIMISIL SCAR GEL?
DIMISIL SCAR GEL is a medical device that received FDA 510(k) clearance on 2003-01-23. The listed applicant is Aesthetic and Reconstructive Technologies, Inc.. The 510(k) number is K023678.
When did DIMISIL SCAR GEL receive FDA 510(k) clearance?
DIMISIL SCAR GEL received FDA 510(k) clearance on 2003-01-23, under 510(k) number K023678.
Who is the listed applicant for DIMISIL SCAR GEL?
The FDA 510(k) record lists Aesthetic and Reconstructive Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIMISIL SCAR GEL?
The FDA product code for DIMISIL SCAR GEL is MDA.
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 Aesthetic and Reconstructive 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: MDA)
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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