KQWClass I

Goniometer, Nonpowered

21 CFR 888.1520 / Orthopedic

KQW is the FDA product code for Goniometer, Nonpowered, a class I device type, regulated under 21 CFR 888.1520. As of 2026-09-10, FDA records hold 13 510(k) clearances under this code, the most recent dated 1993-08-02, and no recalls.

Classification record

Product code: KQW
Device name: Goniometer, Nonpowered
Regulation: 21 CFR 888.1520
Device class: Class I
Review panel: Orthopedic
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 13
Ingested recalls: 0

Clearances, product code KQW

By decision year

13 clearances under product code KQW with a decision year between 1976 and 1993, 1980 the highest year at 4.

Show the numbers

510(k) clearances under FDA product code KQW by decision year
Year	Clearances
1976	2
1980	4
1981	2
1983	1
1985	1
1987	1
1990	1
1993	1

Applicants with the most clearances

Product code KQW

Applicants holding the most 510(k) clearances under product code KQW
Applicant	Clearances
Fred Sammons, Inc.	8
Biosearch Medical Products, Inc.	1
Chattanooga Group, Inc.	1
Sgarlato Laboratories, Inc.	1
The Telos Co.	1
Twin City Surgical, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 77 companies shown, in name order