FDA 510(k)

PERITONEAL CYCLER & MANIFOLD SET

K-Number: K772136 · 1977-12-20

Decision Date1977-12-20

Product CodeKDJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

PERITONEAL CYCLER & MANIFOLD SET is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772136. 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 CYCLER & MANIFOLD SET?

PERITONEAL CYCLER & MANIFOLD SET is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Physio-Control Corp.. The 510(k) number is K772136.

When did PERITONEAL CYCLER & MANIFOLD SET receive FDA 510(k) clearance?

PERITONEAL CYCLER & MANIFOLD SET received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772136.

Who is the listed applicant for PERITONEAL CYCLER & MANIFOLD SET?

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

What is the FDA product code for PERITONEAL CYCLER & MANIFOLD SET?

The FDA product code for PERITONEAL CYCLER & MANIFOLD SET 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.