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FDA 510(k)

BMR-16 CLINIC MUSCLE STIMULATOR

K-Number: K840148 · 1984-01-30

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

Device Summary

BMR-16 CLINIC MUSCLE STIMULATOR 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 K840148. 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-16 CLINIC MUSCLE STIMULATOR?

BMR-16 CLINIC MUSCLE STIMULATOR 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 K840148.

When did BMR-16 CLINIC MUSCLE STIMULATOR receive FDA 510(k) clearance?

BMR-16 CLINIC MUSCLE STIMULATOR received FDA 510(k) clearance on 1984-01-30, under 510(k) number K840148.

Who is the listed applicant for BMR-16 CLINIC MUSCLE STIMULATOR?

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-16 CLINIC MUSCLE STIMULATOR?

The FDA product code for BMR-16 CLINIC MUSCLE STIMULATOR 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, E20K840149BMR POWERSTIMK840147BMR-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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