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

Chromatography(Gas), Clinical Use

21 CFR 862.2250 / Clinical Chemistry
FDA source (opens on fda.gov)

KZQ is the FDA product code for Chromatography(Gas), Clinical Use, a class I device type, regulated under 21 CFR 862.2250. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KZQ
Device name
Chromatography(Gas), Clinical Use
Regulation
21 CFR 862.2250
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
12
Ingested recalls
0

Clearances, product code KZQ

By decision year
12 clearances under product code KZQ with a decision year between 1977 and 1987, 1982 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KZQ by decision year
YearClearances
19772
19791
19801
19823
19833
19841
19871

Applicants with the most clearances

Product code KZQ
Applicants holding the most 510(k) clearances under product code KZQ
ApplicantClearances
Revvity Health Sciences, Inc.5
Hewlett-Packard Co.3
Varian Assoc., Inc.2
Peokin-Elmer Corp.1
Trace Analytical1

Companies listing this code with FDA

Companies whose registered establishments list this code

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