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

Tube, Tissue Culture

21 CFR 864.3010 / Pathology
FDA source (opens on fda.gov)

KJG is the FDA product code for Tube, Tissue Culture, a class I device type, regulated under 21 CFR 864.3010. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
KJG
Device name
Tube, Tissue Culture
Regulation
21 CFR 864.3010
Device class
Class I
Review panel
Pathology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
1

Clearances, product code KJG

By decision year
1 clearance under product code KJG with a decision year between 1983 and 1983, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KJG by decision year
YearClearances
19831

Applicants with the most clearances

Product code KJG
Applicants holding the most 510(k) clearances under product code KJG
ApplicantClearances
Corning Medical & Scientific1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 31 companies shown, in name order