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

Shaker/Stirrer

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

JRQ is the FDA product code for Shaker/Stirrer, a class I device type, regulated under 21 CFR 862.2050. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JRQ
Device name
Shaker/Stirrer
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
8
Ingested recalls
0

Clearances, product code JRQ

By decision year
8 clearances under product code JRQ with a decision year between 1977 and 1981, 1981 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code JRQ by decision year
YearClearances
19771
19781
19792
19801
19813

Applicants with the most clearances

Product code JRQ
Applicants holding the most 510(k) clearances under product code JRQ
ApplicantClearances
American Dade2
American Hospital Supply1
Dynatech Corp.1
Maddak, Inc.1
Scientific Manufacturing Industries1
Sysmex Corporation1
Techhnilab Instruments, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 28 companies shown, in name order