FDA 510(k)

CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL.

K-Number: K991968 · 1999-07-30

Decision Date1999-07-30

Product CodeMDA

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL. is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1999-07-30 under 510(k) number K991968. 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 CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL.?

CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL. is a medical device that received FDA 510(k) clearance on 1999-07-30. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K991968.

When did CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL. receive FDA 510(k) clearance?

CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL. received FDA 510(k) clearance on 1999-07-30, under 510(k) number K991968.

Who is the listed applicant for CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL.?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL.?

The FDA product code for CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL. is MDA.

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Other records listing Smith & Nephew, Inc. as applicant

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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.