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

Densitometeric, Protein Fractionation

21 CFR 862.1630 / Clinical Chemistry
FDA source (opens on fda.gov)

JQJ is the FDA product code for Densitometeric, Protein Fractionation, a class I device type, regulated under 21 CFR 862.1630. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
JQJ
Device name
Densitometeric, Protein Fractionation
Regulation
21 CFR 862.1630
Device class
Class I
Review panel
Clinical Chemistry
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 JQJ

By decision year
1 clearance under product code JQJ with a decision year between 1990 and 1990, 1990 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JQJ by decision year
YearClearances
19901

Applicants with the most clearances

Product code JQJ
Applicants holding the most 510(k) clearances under product code JQJ
ApplicantClearances
Helena Laboratories, Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code