INTRASITE GEL— 510(k) K926508

Substantially Equivalent

Smith & Nephew United, Inc.

FDA 510(k) clearance K926508 for INTRASITE GEL, Substantially Equivalent on 1993-07-13. Applicant: Smith & Nephew United, Inc.. Device class: 1.

Clearance details

Applicant: Smith & Nephew United, Inc.
Product code: Code NAE
Device class: Class 1
Regulation: 21 CFR 878.4022
Advisory panel: General, Plastic Surgery
Date received: 1992-12-30
Decision date: 1993-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Largo, FL, US

Download summary PDF View on FDA.gov ↗

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