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FDA 510(k)

DYNATRON 360 RANGE OF MOTION TESTING DEVICE

K-Number: K897178 · 1990-04-18

ApplicantDynatronics Corp.
Decision Date1990-04-18
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DYNATRON 360 RANGE OF MOTION TESTING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 1990-04-18 under 510(k) number K897178. 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 DYNATRON 360 RANGE OF MOTION TESTING DEVICE?

DYNATRON 360 RANGE OF MOTION TESTING DEVICE is a medical device that received FDA 510(k) clearance on 1990-04-18. The listed applicant is Dynatronics Corp.. The 510(k) number is K897178.

When did DYNATRON 360 RANGE OF MOTION TESTING DEVICE receive FDA 510(k) clearance?

DYNATRON 360 RANGE OF MOTION TESTING DEVICE received FDA 510(k) clearance on 1990-04-18, under 510(k) number K897178.

Who is the listed applicant for DYNATRON 360 RANGE OF MOTION TESTING DEVICE?

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

What is the FDA product code for DYNATRON 360 RANGE OF MOTION TESTING DEVICE?

The FDA product code for DYNATRON 360 RANGE OF MOTION TESTING DEVICE is KQX.

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Other records listing Dynatronics Corp. 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.

K113250DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBEK060814DYNATRON ION IONTOPHORESIS ELECTRODEK051680DYNATRON DX2 TRACTION UNITK051261DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBEK043047DYNATRON IBOX IONTOPHORESIS DEVICEK040729SOLARIS D890 THERAPY PROBE

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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

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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