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

Molybdenum Blue Method, Phospholipids

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

CEQ is the FDA product code for Molybdenum Blue Method, Phospholipids, a class I device type, regulated under 21 CFR 862.1575. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
CEQ
Device name
Molybdenum Blue Method, 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
1
Ingested recalls
0

Clearances, product code CEQ

By decision year
1 clearance under product code CEQ with a decision year between 1986 and 1986, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CEQ by decision year
YearClearances
19861

Applicants with the most clearances

Product code CEQ
Applicants holding the most 510(k) clearances under product code CEQ
ApplicantClearances
J. D. Assoc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code CEQ.