INQClass I

Table, Powered

21 CFR 890.3760 / Physical Medicine

INQ is the FDA product code for Table, Powered, a class I device type, regulated under 21 CFR 890.3760. As of 2026-09-10, FDA records hold 102 510(k) clearances under this code, the most recent dated 1996-02-13, and 2 recalls.

Classification record

Product code: INQ
Device name: Table, Powered
Regulation: 21 CFR 890.3760
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: 102
Ingested recalls: 2

Clearances, product code INQ

By decision year

102 clearances under product code INQ with a decision year between 1977 and 1996, 1995 the highest year at 30.

Show the numbers

510(k) clearances under FDA product code INQ by decision year
Year	Clearances
1977	1
1981	1
1982	2
1983	6
1984	4
1985	4
1986	3
1987	1
1988	1
1989	2
1990	4
1991	2
1992	7
1993	21
1994	9
1995	30
1996	4

Applicants with the most clearances

Product code INQ

Applicants holding the most 510(k) clearances under product code INQ
Applicant	Clearances
Cardon Rehabilitation Products, Inc.	16
Tri W-G, Inc.	14
Hill Laboratories	10
Bailey Mfg. Co.	6
Midland Mfg. Co.	6
Health Care Mfg., Inc.	4
Med Mart, Inc.	4
Medical Device Inspection Company	4
U.S. Table, Inc.	4
S & W Enterprises, Inc.	3

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 53 companies shown, in name order