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FDA 510(k)

KINESTHETICS MODEL 2000 NMS

K-Number: K903870 · 1992-03-13

ApplicantKinesthetics, Inc.
Decision Date1992-03-13
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KINESTHETICS MODEL 2000 NMS is the device name listed in this FDA 510(k) record. The listed applicant is Kinesthetics, Inc.. It received FDA 510(k) clearance on 1992-03-13 under 510(k) number K903870. 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 KINESTHETICS MODEL 2000 NMS?

KINESTHETICS MODEL 2000 NMS is a medical device that received FDA 510(k) clearance on 1992-03-13. The listed applicant is Kinesthetics, Inc.. The 510(k) number is K903870.

When did KINESTHETICS MODEL 2000 NMS receive FDA 510(k) clearance?

KINESTHETICS MODEL 2000 NMS received FDA 510(k) clearance on 1992-03-13, under 510(k) number K903870.

Who is the listed applicant for KINESTHETICS MODEL 2000 NMS?

The FDA 510(k) record lists Kinesthetics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KINESTHETICS MODEL 2000 NMS?

The FDA product code for KINESTHETICS MODEL 2000 NMS is IPF.

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Related Devices (Code: 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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