Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CICACARE MANAGEMENT FOR SCARS

K-Number: K991957 · 1999-07-20

Decision Date1999-07-20
Product CodeMDA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CICACARE MANAGEMENT FOR SCARS 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 1999-07-20 under 510(k) number K991957. 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 MANAGEMENT FOR SCARS?

CICACARE MANAGEMENT FOR SCARS is a medical device that received FDA 510(k) clearance on 1999-07-20. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K991957.

When did CICACARE MANAGEMENT FOR SCARS receive FDA 510(k) clearance?

CICACARE MANAGEMENT FOR SCARS received FDA 510(k) clearance on 1999-07-20, under 510(k) number K991957.

Who is the listed applicant for CICACARE MANAGEMENT FOR SCARS?

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 MANAGEMENT FOR SCARS?

The FDA product code for CICACARE MANAGEMENT FOR SCARS 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 Smith & Nephew, 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.

View all 509 devices →

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.

↑