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FDA 510(k)

PERITONEAL DIALYSIS SYSTEM

K-Number: K760724 · 1976-11-23

ApplicantPhysio-Control Corp.
Decision Date1976-11-23
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERITONEAL DIALYSIS SYSTEM 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 1976-11-23 under 510(k) number K760724. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERITONEAL DIALYSIS SYSTEM?

PERITONEAL DIALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1976-11-23. The listed applicant is Physio-Control Corp.. The 510(k) number is K760724.

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

PERITONEAL DIALYSIS SYSTEM received FDA 510(k) clearance on 1976-11-23, under 510(k) number K760724.

Who is the listed applicant for PERITONEAL DIALYSIS SYSTEM?

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 DIALYSIS SYSTEM?

The FDA product code for PERITONEAL DIALYSIS SYSTEM is EKX.

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Other records listing Physio-Control 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.

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Related Devices (Code: EKX)

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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.

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