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

Peritoneal Dialysate Filter

21 CFR 876.5630 / Gastroenterology, Urology
FDA source (opens on fda.gov)

KPP is the FDA product code for Peritoneal Dialysate Filter, a class II device type, regulated under 21 CFR 876.5630. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KPP
Device name
Peritoneal Dialysate Filter
Regulation
21 CFR 876.5630
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
3
Ingested recalls
0

Clearances, product code KPP

By decision year
3 clearances under product code KPP with a decision year between 1980 and 1982, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KPP by decision year
YearClearances
19801
19811
19821

Applicants with the most clearances

Product code KPP
Applicants holding the most 510(k) clearances under product code KPP
ApplicantClearances
Liquid Crystal Products, Inc.1
EMD Millipore Corporation1
Tri-Med, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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