CURAD SCAR THERAPY
K-Number: K024057 · 2003-06-18
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Device Summary
Frequently Asked Questions
What is the CURAD SCAR THERAPY?
CURAD SCAR THERAPY is a medical device that received FDA 510(k) clearance on 2003-06-18. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K024057.
When did CURAD SCAR THERAPY receive FDA 510(k) clearance?
CURAD SCAR THERAPY received FDA 510(k) clearance on 2003-06-18, under 510(k) number K024057.
Who is the listed applicant for CURAD SCAR THERAPY?
The FDA 510(k) record lists Beiersdorf, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CURAD SCAR THERAPY?
The FDA product code for CURAD SCAR THERAPY 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 Beiersdorf, 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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