ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620)— 510(k) K023429

Name: FDA 510(k) clearance K023429
Creator: U.S. Food and Drug Administration
Published: 2003-09-23

Substantially Equivalent

Rowenta, Inc.

FDA 510(k) clearance K023429 for ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620), Substantially Equivalent on 2003-09-23. Applicant: Rowenta, Inc.. Device class: 2.

Clearance details

Applicant: Rowenta, Inc.
Product code: Code MNW
Device class: Class 2
Regulation: 21 CFR 870.2770
Advisory panel: Cardiovascular
Date received: 2002-10-11
Decision date: 2003-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Medford, MA, US

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