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

Electrode, Ion Selective (Non-Specified)

21 CFR 862.2050 / Clinical Chemistry
FDA source (opens on fda.gov)

JJP is the FDA product code for Electrode, Ion Selective (Non-Specified), a class I device type, regulated under 21 CFR 862.2050. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JJP
Device name
Electrode, Ion Selective (Non-Specified)
Regulation
21 CFR 862.2050
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code JJP

By decision year
3 clearances under product code JJP with a decision year between 1986 and 1990, 1986 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JJP by decision year
YearClearances
19862
19901

Applicants with the most clearances

Product code JJP
Applicants holding the most 510(k) clearances under product code JJP
ApplicantClearances
Amicon, Inc.1
Nova Biomedical Corporation1
Reagent Laboratory, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 14 companies shown, in name order