510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
JXCClass I

Kit, Screening, Yeast

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

JXC is the FDA product code for Kit, Screening, Yeast, a class I device type, regulated under 21 CFR 866.2660. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JXC
Device name
Kit, Screening, Yeast
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
6
Ingested recalls
0

Clearances, product code JXC

By decision year
6 clearances under product code JXC with a decision year between 1983 and 1996, 1989 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JXC by decision year
YearClearances
19831
19881
19892
19921
19961

Applicants with the most clearances

Product code JXC
Applicants holding the most 510(k) clearances under product code JXC
ApplicantClearances
Abbott Medical1
Carr-Scarborough Microbiologicals, Inc.1
Hardy Diagnostics1
Jrga Diagnostics1
Remel Inc1
The Cancer Center at Wadley Institutes1

Companies listing this code with FDA

Companies whose registered establishments list this code