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FDA 510(k)

SILK*SKIN SCAR TREATMENT

K-Number: K953420 · 1995-09-26

ApplicantSilk*Skin Care Co.
Decision Date1995-09-26
Product CodeMDA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SILK*SKIN SCAR TREATMENT is the device name listed in this FDA 510(k) record. The listed applicant is Silk*Skin Care Co.. It received FDA 510(k) clearance on 1995-09-26 under 510(k) number K953420. The device is classified under product code MDA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILK*SKIN SCAR TREATMENT?

SILK*SKIN SCAR TREATMENT is a medical device that received FDA 510(k) clearance on 1995-09-26. The listed applicant is Silk*Skin Care Co.. The 510(k) number is K953420.

When did SILK*SKIN SCAR TREATMENT receive FDA 510(k) clearance?

SILK*SKIN SCAR TREATMENT received FDA 510(k) clearance on 1995-09-26, under 510(k) number K953420.

Who is the listed applicant for SILK*SKIN SCAR TREATMENT?

The FDA 510(k) record lists Silk*Skin Care Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILK*SKIN SCAR TREATMENT?

The FDA product code for SILK*SKIN SCAR TREATMENT is MDA.

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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.

K112131NEODYNE DRESSINGNeodyne Biosciences, Inc.K111733CORELEADER SCAR-DIMMERCoreleader Biotech Co., Ltd.K083718BEAU RX SCAR CARE GELBeau RX Solutions, LLCK053481KELO-COTE SPRAYAdvanced Bio-Technologies, Inc.K041704NEWGEL AND NEWGEL PLUS ENewmedical Technology, Inc.K040307HANSON SCAR ADEHanson Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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