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FDA 510(k)

IMT ULTRASONIC STRIDE MONITOR

K-Number: K854194 · 1986-05-02

Decision Date1986-05-02
Product Code
DecisionSubstantially Equivalent

Device Summary

IMT ULTRASONIC STRIDE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Technologies, Inc.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K854194. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMT ULTRASONIC STRIDE MONITOR?

IMT ULTRASONIC STRIDE MONITOR is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Innovative Medical Technologies, Inc.. The 510(k) number is K854194.

When did IMT ULTRASONIC STRIDE MONITOR receive FDA 510(k) clearance?

IMT ULTRASONIC STRIDE MONITOR received FDA 510(k) clearance on 1986-05-02, under 510(k) number K854194.

Who is the listed applicant for IMT ULTRASONIC STRIDE MONITOR?

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

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.

Other records listing Innovative Medical Technologies, Inc. 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.

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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