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

Culture Media, Antimycobacteria, Susceptibility Test

21 CFR 866.1700 / Microbiology
FDA source (opens on fda.gov)

MJD is the FDA product code for Culture Media, Antimycobacteria, Susceptibility Test, a class II device type, regulated under 21 CFR 866.1700. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MJD
Device name
Culture Media, Antimycobacteria, Susceptibility Test
Regulation
21 CFR 866.1700
Device class
Class II
Review panel
Microbiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
3
Ingested recalls
0

Clearances, product code MJD

By decision year
3 clearances under product code MJD with a decision year between 1983 and 1992, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MJD by decision year
YearClearances
19831
19841
19921

Applicants with the most clearances

Product code MJD
Applicants holding the most 510(k) clearances under product code MJD
ApplicantClearances
Gibco Laboratories Life Technologies, Inc.1
Remel Co.1
Remel Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code