510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
CJDClass II

Nitrosalicylate Reduction, Amylase

21 CFR 862.1070 / Clinical Chemistry
FDA source (opens on fda.gov)

CJD is the FDA product code for Nitrosalicylate Reduction, Amylase, a class II device type, regulated under 21 CFR 862.1070. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
CJD
Device name
Nitrosalicylate Reduction, Amylase
Regulation
21 CFR 862.1070
Device class
Class II
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
1
Ingested recalls
0

Clearances, product code CJD

By decision year
1 clearance under product code CJD with a decision year between 1996 and 1996, 1996 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CJD by decision year
YearClearances
19961

Applicants with the most clearances

Product code CJD
Applicants holding the most 510(k) clearances under product code CJD
ApplicantClearances
Tech Intl. Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code CJD.