SOLOSITE DERMAL WOUND GEL— 510(k) K932263

Substantially Equivalent

Smith & Nephew United, Inc.

FDA 510(k) clearance K932263 for SOLOSITE DERMAL WOUND GEL, Substantially Equivalent on 1993-10-01. Applicant: Smith & Nephew United, Inc..

Clearance details

Applicant: Smith & Nephew United, Inc.
Product code: Code MGQ
Advisory panel: Unknown
Date received: 1993-04-20
Decision date: 1993-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Largo, FL, US

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Adverse events under product code MGQ

product code MGQ

Death: 16
Total: 16

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.