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

Culture Media, Anaerobic Transport

21 CFR 866.2390 / Microbiology
FDA source (opens on fda.gov)

JSL is the FDA product code for Culture Media, Anaerobic Transport, a class I device type, regulated under 21 CFR 866.2390. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JSL
Device name
Culture Media, Anaerobic Transport
Regulation
21 CFR 866.2390
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 JSL

By decision year
8 clearances under product code JSL with a decision year between 1977 and 1997, 1977 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JSL by decision year
YearClearances
19772
19842
19931
19951
19972

Applicants with the most clearances

Product code JSL
Applicants holding the most 510(k) clearances under product code JSL
ApplicantClearances
Anaerobe Systems2
Copan Italia2
Gibco Laboratories Life Technologies, Inc.2
Skoug Research Corp.1
Starplex Scientific Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code