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

Digoxin Control Serum, Ria

21 CFR 862.3280 / Clinical Toxicology
FDA source (opens on fda.gov)

DMP is the FDA product code for Digoxin Control Serum, Ria, a class I device type, regulated under 21 CFR 862.3280. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DMP
Device name
Digoxin Control Serum, Ria
Regulation
21 CFR 862.3280
Device class
Class I
Review panel
Clinical Toxicology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
0

Clearances, product code DMP

By decision year
4 clearances under product code DMP with a decision year between 1977 and 1997, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DMP by decision year
YearClearances
19771
19781
19951
19971

Applicants with the most clearances

Product code DMP
Applicants holding the most 510(k) clearances under product code DMP
ApplicantClearances
Boehringer Mannheim Corp.1
Chimera Research & Chemical, Inc.1
Nuclear Medical Laboratories, Inc.1
Pcl-Ria, 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 DMP.