Community Balance Performance Monitor or Community BPM

FDA 510(k) K951771 · Sms Technologies, Ltd.

Substantially Equivalent

510(k) numberK951771

Submission

Device name
Community Balance Performance Monitor or Community BPM
Applicant
Sms Technologies, Ltd.
Harlow, Essex, GB
Received
April 17, 1995
Decision date
August 11, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KHX – Platform, Force-Measuring
Device class
Class I (low risk)
Regulation
21 CFR 890.1575
Specialty
Physical Medicine

Other 510(k)s with product code KHX

510(k)DeviceApplicantDecision
K946229Balance ManagerKHX · Traditional Neurocom International, Inc.08/04/1995SE
K942694Stability System (110V) Model 945-300; Stability System (220V) Model #945-302KHX · Traditional Biodex Medical Systems, Inc.03/10/1995SE
K930089SMS Balance Performance MonitorKHX · Traditional Sms Technologies, Ltd.06/08/1993SE
K921340Force Measuring PlatformKHX · Traditional Sra Intl., Inc.05/26/1992SE
K901069Computerized Functional Testing Gait SystemKHX · Traditional Computerized Functional Testing Corp.03/16/1990SE
K893254Dynamic System Computerized Podiatric AnalyzerKHX · Traditional Dalphi, Inc.01/02/1990SE
K883198Biovec Biomechanic Force Analysis SystemKHX · Traditional Advanced Mechanical Technology, Inc.10/24/1988SE
K883131Biomechanics Force Platform #LG6-4-1000 & 2000KHX · Traditional Advanced Mechanical Technology, Inc.10/24/1988SE
K883130Biomechanics Force Platform/# OR6-5-1000 & 2000KHX · Traditional Advanced Mechanical Technology, Inc.10/24/1988SE
K883129Biomechanics Force Platform/#Or 6-6-1000 & 2000KHX · Traditional Advanced Mechanical Technology, Inc.10/24/1988SE

More from Advanced Mechanical Technology, Inc.

510(k)DeviceDecision
K930089SMS Balance Performance MonitorKHX · Traditional 06/08/1993SE

Questions and answers

When was Community Balance Performance Monitor or Community BPM cleared by the FDA?

Community Balance Performance Monitor or Community BPM (K951771) received a 510(k) decision of Substantially Equivalent on August 11, 1995, 116 days after the submission was received.

What is the product code of K951771?

The FDA product code is KHX – Platform, Force-Measuring, a Class I (low risk) device regulated under 21 CFR 890.1575.