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

Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin

21 CFR 862.1795 / Clinical Chemistry
FDA source (opens on fda.gov)

CDF is the FDA product code for Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin, a class I device type, regulated under 21 CFR 862.1795. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CDF
Device name
Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin
Regulation
21 CFR 862.1795
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
12
Ingested recalls
0

Clearances, product code CDF

By decision year
12 clearances under product code CDF with a decision year between 1977 and 1996, 1986 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code CDF by decision year
YearClearances
19771
19791
19811
19841
19851
19862
19871
19892
19941
19961

Applicants with the most clearances

Product code CDF
Applicants holding the most 510(k) clearances under product code CDF
ApplicantClearances
Bio-Rad3
Yamasa Shoy Co., Ltd.2
Beckman Instruments, Inc.1
Diagnostic Chemicals, Ltd. (USA)1
Eppendorf-Brinkmann, Inc.1
Esa, Inc.1
German American Chamber of Commerce, Inc.1
Helena Laboratories, Corp.1
Sterling Diagnostics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code