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

Reagents, Cysticercosis

21 CFR 866.3200 / Microbiology
FDA source (opens on fda.gov)

MDJ is the FDA product code for Reagents, Cysticercosis, a class I device type, regulated under 21 CFR 866.3200. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MDJ
Device name
Reagents, Cysticercosis
Regulation
21 CFR 866.3200
Device class
Class I
Review panel
Microbiology
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 MDJ

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

Applicants with the most clearances

Product code MDJ
Applicants holding the most 510(k) clearances under product code MDJ
ApplicantClearances
Lmd Laboratories1

Companies listing this code with FDA

Companies whose registered establishments list this code