BIOMOVE 5000 SYSTEM— 510(k) K080787

Substantially Equivalent

Curatronic, Ltd.

FDA 510(k) clearance K080787 for BIOMOVE 5000 SYSTEM, Substantially Equivalent on 2008-04-17. Applicant: Curatronic, Ltd.. Device class: 2.

Clearance details

Applicant: Curatronic, Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2008-03-20
Decision date: 2008-04-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Kfar Saba, IL

Download summary PDF View on FDA.gov ↗

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