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

1-Nitroso-2-Naphthol (Fluorometric), Free Tyrosine

21 CFR 862.1730 / Clinical Chemistry
FDA source (opens on fda.gov)

CDR is the FDA product code for 1-Nitroso-2-Naphthol (Fluorometric), Free Tyrosine, a class I device type, regulated under 21 CFR 862.1730. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
CDR
Device name
1-Nitroso-2-Naphthol (Fluorometric), Free Tyrosine
Regulation
21 CFR 862.1730
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code CDR

By decision year
1 clearance under product code CDR with a decision year between 1998 and 1998, 1998 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CDR by decision year
YearClearances
19981

Applicants with the most clearances

Product code CDR
Applicants holding the most 510(k) clearances under product code CDR
ApplicantClearances
Astoria-Pacific, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code