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

Transport Systems, Anaerobic

21 CFR 866.2900 / Microbiology
FDA source (opens on fda.gov)

JTX is the FDA product code for Transport Systems, Anaerobic, a class I device type, regulated under 21 CFR 866.2900. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JTX
Device name
Transport Systems, Anaerobic
Regulation
21 CFR 866.2900
Device class
Class I
Review panel
Microbiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
8
Ingested recalls
0

Clearances, product code JTX

By decision year
8 clearances under product code JTX with a decision year between 1976 and 1990, 1976 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JTX by decision year
YearClearances
19762
19782
19791
19881
19902

Applicants with the most clearances

Product code JTX
Applicants holding the most 510(k) clearances under product code JTX
ApplicantClearances
Accu-Med Corp.1
Acuson Corp.1
American Monitor Corp.1
BD Becton Dickinson Vacutainer Systems Preanalytic1
Gibco Laboratories Life Technologies, Inc.1
Marion Laboratories, Inc.1
Medical Laboratory Automation Systems, Inc.1
Scott Laboratories, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code