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

Dna Probe, Gardnerella Vaginalis

21 CFR 866.2660 / Microbiology
FDA source (opens on fda.gov)

MJM is the FDA product code for Dna Probe, Gardnerella Vaginalis, a class I device type, regulated under 21 CFR 866.2660. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MJM
Device name
Dna Probe, Gardnerella Vaginalis
Regulation
21 CFR 866.2660
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
2
Ingested recalls
0

Clearances, product code MJM

By decision year
2 clearances under product code MJM with a decision year between 1992 and 1997, 1992 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MJM by decision year
YearClearances
19921
19971

Applicants with the most clearances

Product code MJM
Applicants holding the most 510(k) clearances under product code MJM
ApplicantClearances
Litmus Concepts, Inc.1
Microprobe Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code