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FDA 510(k)

BMR POWERSTIM

K-Number: K840149 · 1984-01-30

ApplicantBio-Medical Research Corp.
Decision Date1984-01-30
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BMR POWERSTIM is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Medical Research Corp.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K840149. 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 BMR POWERSTIM?

BMR POWERSTIM is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Bio-Medical Research Corp.. The 510(k) number is K840149.

When did BMR POWERSTIM receive FDA 510(k) clearance?

BMR POWERSTIM received FDA 510(k) clearance on 1984-01-30, under 510(k) number K840149.

Who is the listed applicant for BMR POWERSTIM?

The FDA 510(k) record lists Bio-Medical Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BMR POWERSTIM?

The FDA product code for BMR POWERSTIM is IPF.

Related Clinical Trials

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.

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Other records listing Bio-Medical Research 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.

K071666SLENDERTONE ENERVIVE, MODEL 561K070142SLENDERTONE SYSTEM ABS, MODELS 390, E10, X10; SLENDERTONE SYSTEM SHORTS, MODELS 390, E20K840148BMR-16 CLINIC MUSCLE STIMULATORK840147BMR-2 MUSCLE STIMULATOR

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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