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

Monitor, Microbial Growth

21 CFR 866.2560 / Microbiology
FDA source (opens on fda.gov)

JTA is the FDA product code for Monitor, Microbial Growth, a class I device type, regulated under 21 CFR 866.2560. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JTA
Device name
Monitor, Microbial Growth
Regulation
21 CFR 866.2560
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
11
Ingested recalls
0

Clearances, product code JTA

By decision year
11 clearances under product code JTA with a decision year between 1979 and 1996, 1984 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code JTA by decision year
YearClearances
19792
19811
19844
19851
19871
19911
19961

Applicants with the most clearances

Product code JTA
Applicants holding the most 510(k) clearances under product code JTA
ApplicantClearances
BD Becton Dickinson Vacutainer Systems Preanalytic6
Abbott Medical1
American Micro Scan1
Applied Polytechnology, Inc.1
Becton Dickinson Diagnostic Instrument Systems1
Marion Laboratories, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code