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

Nephelometric Method, Lipoproteins

21 CFR 862.1475 / Clinical Chemistry
FDA source (opens on fda.gov)

JHQ is the FDA product code for Nephelometric Method, Lipoproteins, a class I device type, regulated under 21 CFR 862.1475. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
JHQ
Device name
Nephelometric Method, Lipoproteins
Regulation
21 CFR 862.1475
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 JHQ

By decision year
1 clearance under product code JHQ with a decision year between 1981 and 1981, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JHQ by decision year
YearClearances
19811

Applicants with the most clearances

Product code JHQ
Applicants holding the most 510(k) clearances under product code JHQ
ApplicantClearances
Syn-Kit, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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