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

Polarimeter

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

JQZ is the FDA product code for Polarimeter, a class I device type, regulated under 21 CFR 862.2050. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
JQZ
Device name
Polarimeter
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
1
Ingested recalls
0

Clearances, product code JQZ

By decision year
1 clearance under product code JQZ with a decision year between 1981 and 1981, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JQZ by decision year
YearClearances
19811

Applicants with the most clearances

Product code JQZ
Applicants holding the most 510(k) clearances under product code JQZ
ApplicantClearances
Abbott Medical1

Companies listing this code with FDA

Companies whose registered establishments list this code