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

Porter Silber Hydrazone, 17-Hydroxycorticosteroids

21 CFR 862.1385 / Clinical Chemistry
FDA source (opens on fda.gov)

CDB is the FDA product code for Porter Silber Hydrazone, 17-Hydroxycorticosteroids, a class I device type, regulated under 21 CFR 862.1385. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CDB
Device name
Porter Silber Hydrazone, 17-Hydroxycorticosteroids
Regulation
21 CFR 862.1385
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
2
Ingested recalls
0

Clearances, product code CDB

By decision year
2 clearances under product code CDB with a decision year between 1977 and 1978, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CDB by decision year
YearClearances
19771
19781

Applicants with the most clearances

Product code CDB
Applicants holding the most 510(k) clearances under product code CDB
ApplicantClearances
Eppendorf-Brinkmann, Inc.1
Hycel, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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