BIOMOVE 3000— 510(k) K042650

Substantially Equivalent

Curatronic, Ltd.

FDA 510(k) clearance K042650 for BIOMOVE 3000, Substantially Equivalent on 2005-01-27. 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: 2004-09-28
Decision date: 2005-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Heshmonayim, IL

Download summary PDF View on FDA.gov ↗

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