FDA 510(k)

PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD

K-Number: K892870 · 1989-05-18

ApplicantNational Medical Care, Medical Products Div., Inc.

Decision Date1989-05-18

Product CodeKDJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is National Medical Care, Medical Products Div., Inc.. It received FDA 510(k) clearance on 1989-05-18 under 510(k) number K892870. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD?

PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD is a medical device that received FDA 510(k) clearance on 1989-05-18. The listed applicant is National Medical Care, Medical Products Div., Inc.. The 510(k) number is K892870.

When did PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD receive FDA 510(k) clearance?

PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD received FDA 510(k) clearance on 1989-05-18, under 510(k) number K892870.

Who is the listed applicant for PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD?

The FDA 510(k) record lists National Medical Care, Medical Products Div., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD?

The FDA product code for PERITONEAL DIALYSIS CYCLER SET, W/5 PRONG MANIFOLD is KDJ.

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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.