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

Microtitrator, For Clinical Use

21 CFR 862.2680 / Clinical Chemistry
FDA source (opens on fda.gov)

JRA is the FDA product code for Microtitrator, For Clinical Use, a class I device type, regulated under 21 CFR 862.2680. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
JRA
Device name
Microtitrator, For Clinical Use
Regulation
21 CFR 862.2680
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
1
Ingested recalls
0

Clearances, product code JRA

By decision year
1 clearance under product code JRA with a decision year between 1997 and 1997, 1997 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JRA by decision year
YearClearances
19971

Applicants with the most clearances

Product code JRA
Applicants holding the most 510(k) clearances under product code JRA
ApplicantClearances
Tecan U.S.1

Companies listing this code with FDA

Companies whose registered establishments list this code