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FDA 510(k)

THE HANDSCAN SYSTEM

K-Number: K893455 · 1989-08-30

ApplicantDigital Body Systems, Inc.
Decision Date1989-08-30
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE HANDSCAN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Digital Body Systems, Inc.. It received FDA 510(k) clearance on 1989-08-30 under 510(k) number K893455. 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 HANDSCAN SYSTEM?

THE HANDSCAN SYSTEM is a medical device that received FDA 510(k) clearance on 1989-08-30. The listed applicant is Digital Body Systems, Inc.. The 510(k) number is K893455.

When did THE HANDSCAN SYSTEM receive FDA 510(k) clearance?

THE HANDSCAN SYSTEM received FDA 510(k) clearance on 1989-08-30, under 510(k) number K893455.

Who is the listed applicant for THE HANDSCAN SYSTEM?

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

What is the FDA product code for THE HANDSCAN SYSTEM?

The FDA product code for THE HANDSCAN SYSTEM is KQX.

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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

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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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