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FDA 510(k)

ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC

K-Number: K850388 · 1985-04-25

ApplicantInstrument Technology, Inc.
Decision Date1985-04-25
Product Code
DecisionSubstantially Equivalent

Device Summary

ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC is the device name listed in this FDA 510(k) record. The listed applicant is Instrument Technology, Inc.. It received FDA 510(k) clearance on 1985-04-25 under 510(k) number K850388. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC?

ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Instrument Technology, Inc.. The 510(k) number is K850388.

When did ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC receive FDA 510(k) clearance?

ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC received FDA 510(k) clearance on 1985-04-25, under 510(k) number K850388.

Who is the listed applicant for ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC?

The FDA 510(k) record lists Instrument Technology, 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.

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Other records listing Instrument Technology, 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.

K852655COMBISCOPE

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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