CUTERA TABLETOP AESTHETIC PRODUCT
K-Number: K042165 · 2004-10-18
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Device Summary
Frequently Asked Questions
What is the CUTERA TABLETOP AESTHETIC PRODUCT?
CUTERA TABLETOP AESTHETIC PRODUCT is a medical device that received FDA 510(k) clearance on 2004-10-18. The listed applicant is Cutera, Inc.. The 510(k) number is K042165.
When did CUTERA TABLETOP AESTHETIC PRODUCT receive FDA 510(k) clearance?
CUTERA TABLETOP AESTHETIC PRODUCT received FDA 510(k) clearance on 2004-10-18, under 510(k) number K042165.
Who is the listed applicant for CUTERA TABLETOP AESTHETIC PRODUCT?
The FDA 510(k) record lists Cutera, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUTERA TABLETOP AESTHETIC PRODUCT?
The FDA product code for CUTERA TABLETOP AESTHETIC PRODUCT is ILY.
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 Cutera, 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: ILY)
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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