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FDA 510(k)

HANDMASTER NMS1

K-Number: K982482 · 1998-09-30

ApplicantN.E.S.S. Nuromuscular Electrical Stimulation Syst
Decision Date1998-09-30
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 N.E.S.S. Nuromuscular Electrical Stimulation Syst. It received FDA 510(k) clearance on 1998-09-30 under 510(k) number K982482. 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 1998-09-30. The listed applicant is N.E.S.S. Nuromuscular Electrical Stimulation Syst. The 510(k) number is K982482.

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

HANDMASTER NMS1 received FDA 510(k) clearance on 1998-09-30, under 510(k) number K982482.

Who is the listed applicant for HANDMASTER NMS1?

The FDA 510(k) record lists N.E.S.S. Nuromuscular Electrical Stimulation Syst 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.

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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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