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

Freezer

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

JRM is the FDA product code for Freezer, a class I device type, regulated under 21 CFR 862.2050. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
JRM
Device name
Freezer
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
7
Ingested recalls
1

Clearances, product code JRM

By decision year
7 clearances under product code JRM with a decision year between 1979 and 1992, 1992 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code JRM by decision year
YearClearances
19791
19891
19911
19924

Applicants with the most clearances

Product code JRM
Applicants holding the most 510(k) clearances under product code JRM
ApplicantClearances
Mnlase, Inc.4
Saniserv, Inc.1
Sherwood Medical Industries1
Taylor Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 21 companies shown, in name order