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

Device, Media Dispensing/Stacking

21 CFR 866.2440 / Microbiology
FDA source (opens on fda.gov)

JTB is the FDA product code for Device, Media Dispensing/Stacking, a class I device type, regulated under 21 CFR 866.2440. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JTB
Device name
Device, Media Dispensing/Stacking
Regulation
21 CFR 866.2440
Device class
Class I
Review panel
Microbiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code JTB

By decision year
2 clearances under product code JTB with a decision year between 1979 and 1980, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JTB by decision year
YearClearances
19791
19801

Applicants with the most clearances

Product code JTB
Applicants holding the most 510(k) clearances under product code JTB
ApplicantClearances
Acacia, Inc.1
Siemens Healthcare Diagnostics Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code