Biovec Biomechanic Force Analysis System

FDA 510(k) K883198 · Advanced Mechanical Technology, Inc.

Substantially Equivalent

510(k) numberK883198

Submission

Device name
Biovec Biomechanic Force Analysis System
Applicant
Advanced Mechanical Technology, Inc.
Newton, CA, US
Received
July 28, 1988
Decision date
October 24, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

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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
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
K883131Biomechanics Force Platform #LG6-4-1000 & 2000KHX · Traditional 10/24/1988SE
K883130Biomechanics Force Platform/# OR6-5-1000 & 2000KHX · Traditional 10/24/1988SE
K883129Biomechanics Force Platform/#Or 6-6-1000 & 2000KHX · Traditional 10/24/1988SE
K883127Multi-Channel Strain-Gage Amplifier & Power SupplyKHX · Traditional 09/30/1988SE

Questions and answers

When was Biovec Biomechanic Force Analysis System cleared by the FDA?

Biovec Biomechanic Force Analysis System (K883198) received a 510(k) decision of Substantially Equivalent on October 24, 1988, 88 days after the submission was received.

What is the product code of K883198?

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