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FDA 510(k)

THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK

K-Number: K925225 · 1994-06-27

ApplicantBaltimore Therapeutic Equipment Co.
Decision Date1994-06-27
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK is the device name listed in this FDA 510(k) record. The listed applicant is Baltimore Therapeutic Equipment Co.. It received FDA 510(k) clearance on 1994-06-27 under 510(k) number K925225. 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 BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK?

THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK is a medical device that received FDA 510(k) clearance on 1994-06-27. The listed applicant is Baltimore Therapeutic Equipment Co.. The 510(k) number is K925225.

When did THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK receive FDA 510(k) clearance?

THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK received FDA 510(k) clearance on 1994-06-27, under 510(k) number K925225.

Who is the listed applicant for THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK?

The FDA 510(k) record lists Baltimore Therapeutic Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK?

The FDA product code for THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK is KQX.

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Other records listing Baltimore Therapeutic Equipment Co. 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.

K955106BTE CPM-20K955105BTE CPM-10K933611THE BTE WS30K924414THE BTE DYNAMIC LIFTK895881MOTIONSPECTK800007WORK SIMULATOR

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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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