510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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CELClass I

Ammonium Molybdate And Ammonium Vanadate, Phospholipids

21 CFR 862.1575 / Clinical Chemistry
FDA source (opens on fda.gov)

CEL is the FDA product code for Ammonium Molybdate And Ammonium Vanadate, Phospholipids, a class I device type, regulated under 21 CFR 862.1575. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CEL
Device name
Ammonium Molybdate And Ammonium Vanadate, Phospholipids
Regulation
21 CFR 862.1575
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
3
Ingested recalls
0

Clearances, product code CEL

By decision year
3 clearances under product code CEL with a decision year between 1980 and 1991, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CEL by decision year
YearClearances
19801
19891
19911

Applicants with the most clearances

Product code CEL
Applicants holding the most 510(k) clearances under product code CEL
ApplicantClearances
Kamiya Biomedical Company, LLC1
The du Pont Co.1
Wako Pure Chemical Industries, Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code