ARTIFLEX(TM)— 510(k) K910274

Substantially Equivalent

Beiersdorf, Inc.

FDA 510(k) clearance K910274 for ARTIFLEX(TM), Substantially Equivalent on 1991-03-05. Applicant: Beiersdorf, Inc.. Device class: 1.

Clearance details

Applicant: Beiersdorf, Inc.
Product code: Code LGF
Device class: Class 1
Regulation: 21 CFR 888.5940
Advisory panel: Orthopedic
Date received: 1991-01-23
Decision date: 1991-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

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