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

Atomic Absorption Spectrophotometer, General Use

21 CFR 862.2850 / Clinical Chemistry
FDA source (opens on fda.gov)

JXR is the FDA product code for Atomic Absorption Spectrophotometer, General Use, a class I device type, regulated under 21 CFR 862.2850. As of , FDA records hold 29 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JXR
Device name
Atomic Absorption Spectrophotometer, General Use
Regulation
21 CFR 862.2850
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
29
Ingested recalls
0

Clearances, product code JXR

By decision year
29 clearances under product code JXR with a decision year between 1976 and 1990, 1977 the highest year at 7.
Show the numbers
510(k) clearances under FDA product code JXR by decision year
YearClearances
19761
19777
19786
19797
19801
19811
19821
19831
19842
19881
19901

Applicants with the most clearances

Product code JXR
Applicants holding the most 510(k) clearances under product code JXR
ApplicantClearances
Revvity Health Sciences, Inc.17
Varian Assoc., Inc.6
Instrumentation Laboratory Co.5
Ciba Corning Diagnostics Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code JXR.