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FDA 510(k)

ELECTRONIC MUSCLE MASSAGE, MODELS BE-550 AND BE-660

K-Number: K031820 · 2003-11-12

ApplicantMultinational
Decision Date2003-11-12
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC MUSCLE MASSAGE, MODELS BE-550 AND BE-660 is the device name listed in this FDA 510(k) record. The listed applicant is Multinational. It received FDA 510(k) clearance on 2003-11-12 under 510(k) number K031820. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRONIC MUSCLE MASSAGE, MODELS BE-550 AND BE-660?

ELECTRONIC MUSCLE MASSAGE, MODELS BE-550 AND BE-660 is a medical device that received FDA 510(k) clearance on 2003-11-12. The listed applicant is Multinational. The 510(k) number is K031820.

When did ELECTRONIC MUSCLE MASSAGE, MODELS BE-550 AND BE-660 receive FDA 510(k) clearance?

ELECTRONIC MUSCLE MASSAGE, MODELS BE-550 AND BE-660 received FDA 510(k) clearance on 2003-11-12, under 510(k) number K031820.

Who is the listed applicant for ELECTRONIC MUSCLE MASSAGE, MODELS BE-550 AND BE-660?

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

What is the FDA product code for ELECTRONIC MUSCLE MASSAGE, MODELS BE-550 AND BE-660?

The FDA product code for ELECTRONIC MUSCLE MASSAGE, MODELS BE-550 AND BE-660 is IPF.

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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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