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FDA 510(k)

GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM

K-Number: K893537 · 1989-10-10

ApplicantGreenleaf Medical Systems, Inc.
Decision Date1989-10-10
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM 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 1989-10-10 under 510(k) number K893537. The device is classified under product code LBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM?

GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM is a medical device that received FDA 510(k) clearance on 1989-10-10. The listed applicant is Greenleaf Medical Systems, Inc.. The 510(k) number is K893537.

When did GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM receive FDA 510(k) clearance?

GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM received FDA 510(k) clearance on 1989-10-10, under 510(k) number K893537.

Who is the listed applicant for GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM?

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 GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM?

The FDA product code for GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM is LBB.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)K935757GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEMK884723(DATAGLOVE) HAND IMPAIRMENT EVALUATION SYSTEM

Related Devices (Code: LBB)

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.

K162412Hoggan Scientific® microFET2™Hoggan Scientific, LLCK073154FACTS HAND AND PINCH GRIP COMBOGlobal Services Group, LLCK052309DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH5006Saehan Corp.K042889DYNAMOMETER - MODEL FCE AND MODEL MSCAmetekK012492KADANCE 2000Kada Research, Inc.K981730DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002Nk Biotechnical Corp.

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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