CEOClass I

Phosphomolybdate (Colorimetric), Inorganic Phosphorus

21 CFR 862.1580 / Clinical Chemistry

CEO is the FDA product code for Phosphomolybdate (Colorimetric), Inorganic Phosphorus, a class I device type, regulated under 21 CFR 862.1580. As of 2026-09-10, FDA records hold 105 510(k) clearances under this code, the most recent dated 2011-05-06, and 8 recalls.

Classification record

Product code: CEO
Device name: Phosphomolybdate (Colorimetric), Inorganic Phosphorus
Regulation: 21 CFR 862.1580
Device class: Class I
Review panel: Clinical Chemistry
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 105
Ingested recalls: 8

Clearances, product code CEO

By decision year

105 clearances under product code CEO with a decision year between 1976 and 2011, 1986 the highest year at 9.

Show the numbers

510(k) clearances under FDA product code CEO by decision year
Year	Clearances
1976	5
1977	6
1978	1
1979	4
1980	3
1981	2
1982	2
1983	3
1984	7
1985	7
1986	9
1987	7
1988	5
1989	3
1990	7
1991	3
1992	5
1993	4
1994	3
1995	1
1996	1
1997	1
1998	7
1999	1
2000	1
2001	2
2002	1
2003	1
2004	1
2008	1
2011	1

Applicants with the most clearances

Product code CEO

Applicants holding the most 510(k) clearances under product code CEO
Applicant	Clearances
Em Diagnostic Systems, Inc.	10
Harleco	5
Abbott Medical	4
American Research Products Co.	4
Data Medical Associates, Inc.	3
Olympus Corp.	3
Diagnostic Chemicals, Ltd. (USA)	2
Eastman Kodak Company	2
EMD Millipore Corporation	2
Instrumentation Laboratory Co.	2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 32 companies shown, in name order