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FDA 510(k)

SOLOSITE DERMAL WOUND GEL

K-Number: K932263 · 1993-10-01

ApplicantSmith & Nephew United, Inc.
Decision Date1993-10-01
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

SOLOSITE DERMAL WOUND GEL is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew United, Inc.. It received FDA 510(k) clearance on 1993-10-01 under 510(k) number K932263. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLOSITE DERMAL WOUND GEL?

SOLOSITE DERMAL WOUND GEL is a medical device that received FDA 510(k) clearance on 1993-10-01. The listed applicant is Smith & Nephew United, Inc.. The 510(k) number is K932263.

When did SOLOSITE DERMAL WOUND GEL receive FDA 510(k) clearance?

SOLOSITE DERMAL WOUND GEL received FDA 510(k) clearance on 1993-10-01, under 510(k) number K932263.

Who is the listed applicant for SOLOSITE DERMAL WOUND GEL?

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

What is the FDA product code for SOLOSITE DERMAL WOUND GEL?

The FDA product code for SOLOSITE DERMAL WOUND GEL is MGQ.

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Other records listing Smith & Nephew United, 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.

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