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

Unit, Filter, Membrane

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

JRL is the FDA product code for Unit, Filter, Membrane, a class I device type, regulated under 21 CFR 862.2050. As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JRL
Device name
Unit, Filter, Membrane
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
9
Ingested recalls
0

Clearances, product code JRL

By decision year
9 clearances under product code JRL with a decision year between 1978 and 1982, 1982 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code JRL by decision year
YearClearances
19781
19791
19801
19812
19824

Applicants with the most clearances

Product code JRL
Applicants holding the most 510(k) clearances under product code JRL
ApplicantClearances
Gelman Sciences, Inc.3
EMD Millipore Corporation3
Amicon, Inc.1
Instrumentation Laboratory Co.1
Syva Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 50 companies shown, in name order