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

Tubing, Dialysate (And Connector)

21 CFR 876.5820 / Gastroenterology, Urology
FDA source (opens on fda.gov)

KQQ is the FDA product code for Tubing, Dialysate (And Connector), a class II device type, regulated under 21 CFR 876.5820. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KQQ
Device name
Tubing, Dialysate (And Connector)
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code KQQ

By decision year
1 clearance under product code KQQ with a decision year between 1983 and 1983, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KQQ by decision year
YearClearances
19831

Applicants with the most clearances

Product code KQQ
Applicants holding the most 510(k) clearances under product code KQQ
ApplicantClearances
Steridoc Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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