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

Acid, Nitrous And Nitrosonaphthol, 5-Hydroxyindole Acetic Acid/Serotonin

21 CFR 862.1390 / Clinical Chemistry
FDA source (opens on fda.gov)

CDA is the FDA product code for Acid, Nitrous And Nitrosonaphthol, 5-Hydroxyindole Acetic Acid/Serotonin, a class I device type, regulated under 21 CFR 862.1390. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
CDA
Device name
Acid, Nitrous And Nitrosonaphthol, 5-Hydroxyindole Acetic Acid/Serotonin
Regulation
21 CFR 862.1390
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
1

Clearances, product code CDA

By decision year
3 clearances under product code CDA with a decision year between 1986 and 1995, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CDA by decision year
YearClearances
19861
19901
19951

Applicants with the most clearances

Product code CDA
Applicants holding the most 510(k) clearances under product code CDA
ApplicantClearances
Abbott Medical1
Bio-Rad1
IMMUNOTECH s.r.o.1

Companies listing this code with FDA

Companies whose registered establishments list this code