ELASTOPLAST T.P.N.— 510(k) K831439

Substantially Equivalent

Beiersdorf, Inc.

FDA 510(k) clearance K831439 for ELASTOPLAST T.P.N., Substantially Equivalent on 1983-09-29. Applicant: Beiersdorf, Inc.. Device class: 1.

Clearance details

Applicant: Beiersdorf, Inc.
Product code: Code FPX
Device class: Class 1
Regulation: 21 CFR 880.5240
Advisory panel: General Hospital
Date received: 1983-05-05
Decision date: 1983-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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