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

Lactic Dehydrogenase, Antigen, Antiserum, Control

21 CFR 866.5560 / Immunology
FDA source (opens on fda.gov)

DET is the FDA product code for Lactic Dehydrogenase, Antigen, Antiserum, Control, a class I device type, regulated under 21 CFR 866.5560. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DET
Device name
Lactic Dehydrogenase, Antigen, Antiserum, Control
Regulation
21 CFR 866.5560
Device class
Class I
Review panel
Immunology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code DET

By decision year
1 clearance under product code DET with a decision year between 1990 and 1990, 1990 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DET by decision year
YearClearances
19901

Applicants with the most clearances

Product code DET
Applicants holding the most 510(k) clearances under product code DET
ApplicantClearances
Boehringer Mannheim Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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