FDA 510(k)

DISPOSABLE PERITONEAL DIALYSIS EXTENSION

K-Number: K791722 · 1979-11-16

ApplicantAmerican Medical Products, Inc.

Decision Date1979-11-16

Product CodeKDJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PERITONEAL DIALYSIS EXTENSION is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Products, Inc.. It received FDA 510(k) clearance on 1979-11-16 under 510(k) number K791722. 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 DISPOSABLE PERITONEAL DIALYSIS EXTENSION?

DISPOSABLE PERITONEAL DIALYSIS EXTENSION is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is American Medical Products, Inc.. The 510(k) number is K791722.

When did DISPOSABLE PERITONEAL DIALYSIS EXTENSION receive FDA 510(k) clearance?

DISPOSABLE PERITONEAL DIALYSIS EXTENSION received FDA 510(k) clearance on 1979-11-16, under 510(k) number K791722.

Who is the listed applicant for DISPOSABLE PERITONEAL DIALYSIS EXTENSION?

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

What is the FDA product code for DISPOSABLE PERITONEAL DIALYSIS EXTENSION?

The FDA product code for DISPOSABLE PERITONEAL DIALYSIS EXTENSION is KDJ.

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Official Source

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