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
JJLClass I

Plasma Viscometer For Clinical Use

21 CFR 862.2920 / Clinical Chemistry
FDA source (opens on fda.gov)

JJL is the FDA product code for Plasma Viscometer For Clinical Use, a class I device type, regulated under 21 CFR 862.2920. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
JJL
Device name
Plasma Viscometer For Clinical Use
Regulation
21 CFR 862.2920
Device class
Class I
Review panel
Clinical Chemistry
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 JJL

By decision year
1 clearance under product code JJL with a decision year between 1988 and 1988, 1988 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JJL by decision year
YearClearances
19881

Applicants with the most clearances

Product code JJL
Applicants holding the most 510(k) clearances under product code JJL
ApplicantClearances
Coulter Electronics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code