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FDA 510(k)

DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)

K-Number: K943929 · 1995-05-15

ApplicantGreenleaf Medical Systems, Inc.
Decision Date1995-05-15
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS) is the device name listed in this FDA 510(k) record. The listed applicant is Greenleaf Medical Systems, Inc.. It received FDA 510(k) clearance on 1995-05-15 under 510(k) number K943929. 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 DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)?

DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS) is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is Greenleaf Medical Systems, Inc.. The 510(k) number is K943929.

When did DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS) receive FDA 510(k) clearance?

DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS) received FDA 510(k) clearance on 1995-05-15, under 510(k) number K943929.

Who is the listed applicant for DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)?

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

What is the FDA product code for DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)?

The FDA product code for DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS) is KQX.

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 Greenleaf Medical Systems, 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.

K935757GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEMK893537GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEMK884723(DATAGLOVE) HAND IMPAIRMENT EVALUATION SYSTEM

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.K945630LARGE MUSCLE STRENGTH GAUGEJ-Tech, 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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