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

Device, General Purpose, Hematology

21 CFR 866.6010 / Immunology
FDA source (opens on fda.gov)

LOQ is the FDA product code for Device, General Purpose, Hematology, a class II device type, regulated under 21 CFR 866.6010. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
LOQ
Device name
Device, General Purpose, Hematology
Regulation
21 CFR 866.6010
Device class
Class II
Review panel
Immunology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
1

Clearances, product code LOQ

By decision year
1 clearance under product code LOQ with a decision year between 1998 and 1998, 1998 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LOQ by decision year
YearClearances
19981

Applicants with the most clearances

Product code LOQ
Applicants holding the most 510(k) clearances under product code LOQ
ApplicantClearances
Chiron Diagnostics Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code