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FDA 510(k)

KPP PERITONEAL DIALYSATE FILTER

K-Number: K803275 · 1981-03-13

ApplicantMillipore Corp.
Decision Date1981-03-13
Product CodeKPP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KPP PERITONEAL DIALYSATE FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 1981-03-13 under 510(k) number K803275. The device is classified under product code KPP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KPP PERITONEAL DIALYSATE FILTER?

KPP PERITONEAL DIALYSATE FILTER is a medical device that received FDA 510(k) clearance on 1981-03-13. The listed applicant is Millipore Corp.. The 510(k) number is K803275.

When did KPP PERITONEAL DIALYSATE FILTER receive FDA 510(k) clearance?

KPP PERITONEAL DIALYSATE FILTER received FDA 510(k) clearance on 1981-03-13, under 510(k) number K803275.

Who is the listed applicant for KPP PERITONEAL DIALYSATE FILTER?

The FDA 510(k) record lists Millipore Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KPP PERITONEAL DIALYSATE FILTER?

The FDA product code for KPP PERITONEAL DIALYSATE FILTER is KPP.

Related Clinical Trials

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Other records listing Millipore Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K023892MILLEX VV, GV, AND HV SYRINGE FILTER UNITSK013988MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RK963717MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)K941326ULTRAFREE-CLK934069MILLEX, DUALEX (PLUS, ULTRA)K924347WATERS(TM) 996 PDA

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Related Devices (Code: KPP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K812615TM-CAPDTri-Med, Inc.K800666QUIK-TEMPLiquid Crystal Products, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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