FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK

K Number: K925225 · Decision Jun 27, 1994
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
32
Applicant Total
7
Review Days
619

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Basic Information

Device Name
THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK
K Number
K925225
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.1500
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Baltimore Therapeutic Equipment Co.
Date Received
October 16, 1992
Decision Date
June 27, 1994
Product Code
KQX
Advisory Committee
Orthopedic
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KQX Goniometer, Ac-Powered

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K Number Device Name
K955106 BTE CPM-20
K955105 BTE CPM-10
K933611 THE BTE WS30
K924414 THE BTE DYNAMIC LIFT
K895881 MOTIONSPECT
K800007 WORK SIMULATOR