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

Ninhydrin, Nitrogen (Amino-Nitrogen)

21 CFR 862.1515 / Clinical Chemistry
FDA source (opens on fda.gov)

JMX is the FDA product code for Ninhydrin, Nitrogen (Amino-Nitrogen), a class I device type, regulated under 21 CFR 862.1515. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JMX
Device name
Ninhydrin, Nitrogen (Amino-Nitrogen)
Regulation
21 CFR 862.1515
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
2
Ingested recalls
0

Clearances, product code JMX

By decision year
2 clearances under product code JMX with a decision year between 1978 and 1986, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JMX by decision year
YearClearances
19781
19861

Applicants with the most clearances

Product code JMX
Applicants holding the most 510(k) clearances under product code JMX
ApplicantClearances
Beckman Instruments, Inc.1
Biotecx Laboratories, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code