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

Dna Probe, Trichomonas Vaginalis

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

MJK is the FDA product code for Dna Probe, Trichomonas Vaginalis, a class I device type, regulated under 21 CFR 866.2660. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and 6 recalls.

Classification record

Product code
MJK
Device name
Dna Probe, Trichomonas 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
1
Ingested recalls
6

Clearances, product code MJK

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

Applicants with the most clearances

Product code MJK
Applicants holding the most 510(k) clearances under product code MJK
ApplicantClearances
Microprobe Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code