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
JFSClass II

Coulometric, Chloride

21 CFR 862.1170 / Clinical Chemistry
FDA source (opens on fda.gov)

JFS is the FDA product code for Coulometric, Chloride, a class II device type, regulated under 21 CFR 862.1170. As of , FDA records hold 19 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
JFS
Device name
Coulometric, Chloride
Regulation
21 CFR 862.1170
Device class
Class II
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
19
Ingested recalls
2

Clearances, product code JFS

By decision year
19 clearances under product code JFS with a decision year between 1976 and 2013, 1981 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code JFS by decision year
YearClearances
19761
19771
19782
19792
19803
19814
19822
19831
19871
19921
20131

Applicants with the most clearances

Product code JFS
Applicants holding the most 510(k) clearances under product code JFS
ApplicantClearances
Nobel Scientific Industries, Inc.3
Chem-Elec, Inc.2
Fisher Scientific Company L.L.C.2
Hi Chem, Inc.2
J.T. Baker Chemical Co.2
A-Kem, Inc.1
American Research Products Co.1
Awareness Technology, Inc.1
Bulcher Instruments1
Corning Medical & Scientific1

Companies listing this code with FDA

Companies whose registered establishments list this code