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

Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase

21 CFR 862.3240 / Clinical Toxicology
FDA source (opens on fda.gov)

DLI is the FDA product code for Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase, a class I device type, regulated under 21 CFR 862.3240. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DLI
Device name
Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase
Regulation
21 CFR 862.3240
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
6
Ingested recalls
0

Clearances, product code DLI

By decision year
6 clearances under product code DLI with a decision year between 1977 and 1995, 1986 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code DLI by decision year
YearClearances
19771
19831
19862
19931
19951

Applicants with the most clearances

Product code DLI
Applicants holding the most 510(k) clearances under product code DLI
ApplicantClearances
American Monitor Corp.1
E.I. Dupont de Nemours & Co., Inc.1
Em Diagnostic Systems, Inc.1
Kulzer GmbH1
Sterling Biochemical, Inc.1
Sterling Diagnostics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code