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

Antiserum, Fluorescent, Epstein-Barr Virus

21 CFR 866.3235 / Microbiology
FDA source (opens on fda.gov)

JRY is the FDA product code for Antiserum, Fluorescent, Epstein-Barr Virus, a class I device type, regulated under 21 CFR 866.3235. As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JRY
Device name
Antiserum, Fluorescent, Epstein-Barr Virus
Regulation
21 CFR 866.3235
Device class
Class I
Review panel
Microbiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
9
Ingested recalls
0

Clearances, product code JRY

By decision year
9 clearances under product code JRY with a decision year between 1978 and 2005, 1982 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code JRY by decision year
YearClearances
19781
19811
19823
19892
19901
20051

Applicants with the most clearances

Product code JRY
Applicants holding the most 510(k) clearances under product code JRY
ApplicantClearances
Litton Bionetics2
Zeus Scientific LLC2
Bion Ent., Ltd.1
Biotech Research Laboratories, Inc.1
Gull Laboratories, Inc.1
Hillcrest Biologicals1
Stellar Bio Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code