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FDA 510(k)

BESMED VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, BE-560/BE-580

K-Number: K031375 · 2003-11-20

ApplicantBesmed Health Business Corp
Decision Date2003-11-20
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BESMED VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, BE-560/BE-580 is the device name listed in this FDA 510(k) record. The listed applicant is Besmed Health Business Corp. It received FDA 510(k) clearance on 2003-11-20 under 510(k) number K031375. 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 BESMED VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, BE-560/BE-580?

BESMED VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, BE-560/BE-580 is a medical device that received FDA 510(k) clearance on 2003-11-20. The listed applicant is Besmed Health Business Corp. The 510(k) number is K031375.

When did BESMED VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, BE-560/BE-580 receive FDA 510(k) clearance?

BESMED VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, BE-560/BE-580 received FDA 510(k) clearance on 2003-11-20, under 510(k) number K031375.

Who is the listed applicant for BESMED VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, BE-560/BE-580?

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

What is the FDA product code for BESMED VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, BE-560/BE-580?

The FDA product code for BESMED VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, BE-560/BE-580 is IPF.

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Other records listing Besmed Health Business Corp as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241339Besmed Bacterial Filter and HMEFK172804Besmed Peak Flow MeterK160112Besmed PEEP ValveK091272BESMED JET NEBULIZER BOTTLE SETK031374BESMED VARIOUS MODELS OF TENS, BE-550/BE-660

Related Devices (Code: IPF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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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