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FDA 510(k)

NEOSPORIN SCAR SOLUTION

K-Number: K024160 · 2003-03-17

ApplicantWarner-Lambert Co.
Decision Date2003-03-17
Product CodeMDA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEOSPORIN SCAR SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 2003-03-17 under 510(k) number K024160. 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 NEOSPORIN SCAR SOLUTION?

NEOSPORIN SCAR SOLUTION is a medical device that received FDA 510(k) clearance on 2003-03-17. The listed applicant is Warner-Lambert Co.. The 510(k) number is K024160.

When did NEOSPORIN SCAR SOLUTION receive FDA 510(k) clearance?

NEOSPORIN SCAR SOLUTION received FDA 510(k) clearance on 2003-03-17, under 510(k) number K024160.

Who is the listed applicant for NEOSPORIN SCAR SOLUTION?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEOSPORIN SCAR SOLUTION?

The FDA product code for NEOSPORIN SCAR SOLUTION 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

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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