INTRASITE GEL (LABELING REVISION)— 510(k) K901878

Substantially Equivalent

Smith & Nephew United, Inc.

FDA 510(k) clearance K901878 for INTRASITE GEL (LABELING REVISION), Substantially Equivalent on 1990-06-22. Applicant: Smith & Nephew United, Inc..

Clearance details

Applicant: Smith & Nephew United, Inc.
Product code: Code KMF
Advisory panel: General Hospital
Date received: 1990-04-26
Decision date: 1990-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Largo, FL, US

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