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

Photometric Method, Ammonia

21 CFR 862.1065 / Clinical Chemistry
FDA source (opens on fda.gov)

JID is the FDA product code for Photometric Method, Ammonia, a class I device type, regulated under 21 CFR 862.1065. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
JID
Device name
Photometric Method, Ammonia
Regulation
21 CFR 862.1065
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
4
Ingested recalls
1

Clearances, product code JID

By decision year
4 clearances under product code JID with a decision year between 1981 and 2026, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JID by decision year
YearClearances
19811
19821
19991
20261

Applicants with the most clearances

Product code JID
Applicants holding the most 510(k) clearances under product code JID
ApplicantClearances
Careside, Inc.1
Eastman Kodak Company1
Sequitur Health Corp.1
Wako Pure Chemical Industries, Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code