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

Hemagglutination Inhibition, Morphine

21 CFR 862.3640 / Clinical Toxicology
FDA source (opens on fda.gov)

DLR is the FDA product code for Hemagglutination Inhibition, Morphine, a class II device type, regulated under 21 CFR 862.3640. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DLR
Device name
Hemagglutination Inhibition, Morphine
Regulation
21 CFR 862.3640
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
2
Ingested recalls
0

Clearances, product code DLR

By decision year
2 clearances under product code DLR with a decision year between 1976 and 1979, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DLR by decision year
YearClearances
19761
19791

Applicants with the most clearances

Product code DLR
Applicants holding the most 510(k) clearances under product code DLR
ApplicantClearances
J.T. Baker Chemical Co.1
Technam, 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 DLR.