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

Lipoprotein, High Density, Hdl, Over The Counter

21 CFR 862.1175 / Clinical Chemistry
FDA source (opens on fda.gov)

NAQ is the FDA product code for Lipoprotein, High Density, Hdl, Over The Counter, a class I device type, regulated under 21 CFR 862.1175. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
NAQ
Device name
Lipoprotein, High Density, Hdl, Over The Counter
Regulation
21 CFR 862.1175
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
2
Ingested recalls
1

Clearances, product code NAQ

By decision year
2 clearances under product code NAQ with a decision year between 2000 and 2006, 2000 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NAQ by decision year
YearClearances
20001
20061

Applicants with the most clearances

Product code NAQ
Applicants holding the most 510(k) clearances under product code NAQ
ApplicantClearances
Polymer Technology Systems2

Companies listing this code with FDA

Companies whose registered establishments list this code