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

Radioimmunoassay, Digoxin (3-H), Rabbit Antibody, Charcoal Sep.

21 CFR 862.3320 / Clinical Toxicology
FDA source (opens on fda.gov)

DPD is the FDA product code for Radioimmunoassay, Digoxin (3-H), Rabbit Antibody, Charcoal Sep., a class II device type, regulated under 21 CFR 862.3320. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DPD
Device name
Radioimmunoassay, Digoxin (3-H), Rabbit Antibody, Charcoal Sep.
Regulation
21 CFR 862.3320
Device class
Class II
Review panel
Clinical Toxicology
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 DPD

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

Applicants with the most clearances

Product code DPD
Applicants holding the most 510(k) clearances under product code DPD
ApplicantClearances
MEDLINE INDUSTRIES, LP - Northfield1

Companies listing this code with FDA

Companies whose registered establishments list this code

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