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

Unit, Drying

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

JRJ is the FDA product code for Unit, Drying, 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 3 recalls.

Classification record

Product code
JRJ
Device name
Unit, Drying
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
3

Clearances, product code JRJ

By decision year
1 clearance under product code JRJ with a decision year between 1979 and 1979, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JRJ by decision year
YearClearances
19791

Applicants with the most clearances

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

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 23 companies shown, in name order