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FDA 510(k)

THE ORTHORANGER II ELECTRONIC GONIOMETER

K-Number: K884611 · 1989-01-31

ApplicantMedical Instruments Technology, Inc.
Decision Date1989-01-31
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE ORTHORANGER II ELECTRONIC GONIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instruments Technology, Inc.. It received FDA 510(k) clearance on 1989-01-31 under 510(k) number K884611. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ORTHORANGER II ELECTRONIC GONIOMETER?

THE ORTHORANGER II ELECTRONIC GONIOMETER is a medical device that received FDA 510(k) clearance on 1989-01-31. The listed applicant is Medical Instruments Technology, Inc.. The 510(k) number is K884611.

When did THE ORTHORANGER II ELECTRONIC GONIOMETER receive FDA 510(k) clearance?

THE ORTHORANGER II ELECTRONIC GONIOMETER received FDA 510(k) clearance on 1989-01-31, under 510(k) number K884611.

Who is the listed applicant for THE ORTHORANGER II ELECTRONIC GONIOMETER?

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

What is the FDA product code for THE ORTHORANGER II ELECTRONIC GONIOMETER?

The FDA product code for THE ORTHORANGER II ELECTRONIC GONIOMETER is KQX.

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Other records listing Medical Instruments 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.

K012614KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKINK012640ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDSK012624REPROCESSED ARTHROSCOPIC BLADES, ARTHROSCOPIC SHAVERS, SHAVER BLADE, BLADE, LIMITED REUSE BLADE, ARTHROSCOPIC BURSK012632TOURNIQUET CUFF; PNEUMATIC TOURNIQUET

Related Devices (Code: KQX)

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.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K961212SPINAL TOUCHFasstechK954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, Inc.

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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