FDA 510(k)

CONTINUOUS AMBULATORY DIALYSIS (CAPD)

K-Number: K791512 · 1980-02-06

ApplicantNorton Performance Plastics Corp.

Decision Date1980-02-06

Product CodeKDJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CONTINUOUS AMBULATORY DIALYSIS (CAPD) is the device name listed in this FDA 510(k) record. The listed applicant is Norton Performance Plastics Corp.. It received FDA 510(k) clearance on 1980-02-06 under 510(k) number K791512. 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 CONTINUOUS AMBULATORY DIALYSIS (CAPD)?

CONTINUOUS AMBULATORY DIALYSIS (CAPD) is a medical device that received FDA 510(k) clearance on 1980-02-06. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K791512.

When did CONTINUOUS AMBULATORY DIALYSIS (CAPD) receive FDA 510(k) clearance?

CONTINUOUS AMBULATORY DIALYSIS (CAPD) received FDA 510(k) clearance on 1980-02-06, under 510(k) number K791512.

Who is the listed applicant for CONTINUOUS AMBULATORY DIALYSIS (CAPD)?

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

What is the FDA product code for CONTINUOUS AMBULATORY DIALYSIS (CAPD)?

The FDA product code for CONTINUOUS AMBULATORY DIALYSIS (CAPD) is KDJ.

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Other records listing Norton Performance Plastics Corp. as applicant

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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.