KHXClass I

Platform, Force-Measuring

21 CFR 890.1575 / Physical Medicine

KHX is the FDA product code for Platform, Force-Measuring, a class I device type, regulated under 21 CFR 890.1575. As of 2026-09-10, FDA records hold 15 510(k) clearances under this code, the most recent dated 1995-08-11, and no recalls.

Classification record

Product code: KHX
Device name: Platform, Force-Measuring
Regulation: 21 CFR 890.1575
Device class: Class I
Review panel: Physical Medicine
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 15
Ingested recalls: 0

Clearances, product code KHX

By decision year

15 clearances under product code KHX with a decision year between 1982 and 1995, 1988 the highest year at 5.

Show the numbers

510(k) clearances under FDA product code KHX by decision year
Year	Clearances
1982	2
1986	1
1988	5
1990	2
1992	1
1993	1
1995	3

Applicants with the most clearances

Product code KHX

Applicants holding the most 510(k) clearances under product code KHX
Applicant	Clearances
Advanced Mechanical Technology Inc	5
Neurocom International, Inc.	2
Sms Technologies, Ltd.	2
Sport Medical Technology Inc	1
Computerized Functional Testing Corp.	1
Dalphi, Inc.	1
Medical Equipment Devices, Inc.	1
Sra Intl., Inc.	1
The Langer Group	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 32 companies shown, in name order