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
JCGClass I

Fluid, Diluting, Manual Cell

21 CFR 864.8200 / Hematology
FDA source (opens on fda.gov)

JCG is the FDA product code for Fluid, Diluting, Manual Cell, a class I device type, regulated under 21 CFR 864.8200. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
JCG
Device name
Fluid, Diluting, Manual Cell
Regulation
21 CFR 864.8200
Device class
Class I
Review panel
Hematology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code JCG

By decision year
1 clearance under product code JCG with a decision year between 1989 and 1989, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JCG by decision year
YearClearances
19891

Applicants with the most clearances

Product code JCG
Applicants holding the most 510(k) clearances under product code JCG
ApplicantClearances
Scientific Distributors, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code