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FDA 510(k)

ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)

K-Number: K922550 · 1992-12-10

ApplicantVerimed Holdings, Inc.
Decision Date1992-12-10
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) is the device name listed in this FDA 510(k) record. The listed applicant is Verimed Holdings, Inc.. It received FDA 510(k) clearance on 1992-12-10 under 510(k) number K922550. 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 ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)?

ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) is a medical device that received FDA 510(k) clearance on 1992-12-10. The listed applicant is Verimed Holdings, Inc.. The 510(k) number is K922550.

When did ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) receive FDA 510(k) clearance?

ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) received FDA 510(k) clearance on 1992-12-10, under 510(k) number K922550.

Who is the listed applicant for ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)?

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

What is the FDA product code for ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)?

The FDA product code for ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) is KQX.

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Other records listing Verimed Holdings, 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.

K981277PERIFORMK954127BIOFEEDBACK DEVICEK951969MYOEXORCISER II FUALK930670PHYACTION 787K913912VERIMED PERINEOMETERK893220VERIMED MYOEXORCISER VERISTIM

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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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