PARAGOLFER— 510(k) K060936

Substantially Equivalent

Parabasetec, GmbH

FDA 510(k) clearance K060936 for PARAGOLFER, Substantially Equivalent on 2006-08-07. Applicant: Parabasetec, GmbH. Device class: 2.

Clearance details

Applicant: Parabasetec, GmbH
Product code: Code IPL
Device class: Class 2
Regulation: 21 CFR 890.3900
Advisory panel: Physical Medicine
Date received: 2006-04-05
Decision date: 2006-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St Paul, MN, 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.