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

Fluorometry, Morphine

21 CFR 862.3640 / Clinical Toxicology
FDA source (opens on fda.gov)

DJJ is the FDA product code for Fluorometry, Morphine, a class II device type, regulated under 21 CFR 862.3640. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DJJ
Device name
Fluorometry, Morphine
Regulation
21 CFR 862.3640
Device class
Class II
Review panel
Clinical Toxicology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code DJJ

By decision year
1 clearance under product code DJJ with a decision year between 2001 and 2001, 2001 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DJJ by decision year
YearClearances
20011

Applicants with the most clearances

Product code DJJ
Applicants holding the most 510(k) clearances under product code DJJ
ApplicantClearances
Branan Medical Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code