FDA 510(k)

PERITONEAL DIALYSIS CYCLER MODEL PDC1000

K-Number: K791676 · 1979-12-06

Decision Date1979-12-06

Product CodeKPF

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

PERITONEAL DIALYSIS CYCLER MODEL PDC1000 is the device name listed in this FDA 510(k) record. The listed applicant is J.M. Sounds Electronics Co.. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K791676. The device is classified under product code KPF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERITONEAL DIALYSIS CYCLER MODEL PDC1000?

PERITONEAL DIALYSIS CYCLER MODEL PDC1000 is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is J.M. Sounds Electronics Co.. The 510(k) number is K791676.

When did PERITONEAL DIALYSIS CYCLER MODEL PDC1000 receive FDA 510(k) clearance?

PERITONEAL DIALYSIS CYCLER MODEL PDC1000 received FDA 510(k) clearance on 1979-12-06, under 510(k) number K791676.

Who is the listed applicant for PERITONEAL DIALYSIS CYCLER MODEL PDC1000?

The FDA 510(k) record lists J.M. Sounds Electronics Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERITONEAL DIALYSIS CYCLER MODEL PDC1000?

The FDA product code for PERITONEAL DIALYSIS CYCLER MODEL PDC1000 is KPF.

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Related Devices (Code: KPF)

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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.