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

Kit, Culture, Chromosome

21 CFR 864.2260 / Hematology
FDA source (opens on fda.gov)

KIQ is the FDA product code for Kit, Culture, Chromosome, a class I device type, regulated under 21 CFR 864.2260. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KIQ
Device name
Kit, Culture, Chromosome
Regulation
21 CFR 864.2260
Device class
Class I
Review panel
Hematology
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 KIQ

By decision year
1 clearance under product code KIQ with a decision year between 1979 and 1979, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KIQ by decision year
YearClearances
19791

Applicants with the most clearances

Product code KIQ
Applicants holding the most 510(k) clearances under product code KIQ
ApplicantClearances
Pharmacia Fine Chemicals1

Companies listing this code with FDA

Companies whose registered establishments list this code