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FDA 510(k)

HANDMASTER NMS1

K-Number: K952273 · 1996-05-23

ApplicantNeuromusclar Electrical Stimulation Systems, Ltd.
Decision Date1996-05-23
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HANDMASTER NMS1 is the device name listed in this FDA 510(k) record. The listed applicant is Neuromusclar Electrical Stimulation Systems, Ltd.. It received FDA 510(k) clearance on 1996-05-23 under 510(k) number K952273. 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 HANDMASTER NMS1?

HANDMASTER NMS1 is a medical device that received FDA 510(k) clearance on 1996-05-23. The listed applicant is Neuromusclar Electrical Stimulation Systems, Ltd.. The 510(k) number is K952273.

When did HANDMASTER NMS1 receive FDA 510(k) clearance?

HANDMASTER NMS1 received FDA 510(k) clearance on 1996-05-23, under 510(k) number K952273.

Who is the listed applicant for HANDMASTER NMS1?

The FDA 510(k) record lists Neuromusclar Electrical Stimulation Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HANDMASTER NMS1?

The FDA product code for HANDMASTER NMS1 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 Neuromusclar Electrical Stimulation Systems, Ltd. 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.

K010837HANDMASTER

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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