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FDA 510(k)

ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620)

K-Number: K023429 · 2003-09-23

ApplicantRowenta, Inc.
Decision Date2003-09-23
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620) is the device name listed in this FDA 510(k) record. The listed applicant is Rowenta, Inc.. It received FDA 510(k) clearance on 2003-09-23 under 510(k) number K023429. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620)?

ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620) is a medical device that received FDA 510(k) clearance on 2003-09-23. The listed applicant is Rowenta, Inc.. The 510(k) number is K023429.

When did ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620) receive FDA 510(k) clearance?

ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620) received FDA 510(k) clearance on 2003-09-23, under 510(k) number K023429.

Who is the listed applicant for ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620)?

The FDA 510(k) record lists Rowenta, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620)?

The FDA product code for ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620) is MNW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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