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

Plates, Ouchterlony Agar

21 CFR 866.4600 / Immunology
FDA source (opens on fda.gov)

JZP is the FDA product code for Plates, Ouchterlony Agar, a class I device type, regulated under 21 CFR 866.4600. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
JZP
Device name
Plates, Ouchterlony Agar
Regulation
21 CFR 866.4600
Device class
Class I
Review panel
Immunology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code JZP

By decision year
1 clearance under product code JZP with a decision year between 1976 and 1976, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JZP by decision year
YearClearances
19761

Applicants with the most clearances

Product code JZP
Applicants holding the most 510(k) clearances under product code JZP
ApplicantClearances
Behring Diagnostics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code