PERITONEAL DIALYSIS CYCLER MODEL PDC1000— 510(k) K791676

Name: FDA 510(k) clearance K791676
Creator: U.S. Food and Drug Administration
Published: 1979-12-06

Substantially Equivalent

J.M. Sounds Electronics Co.

FDA 510(k) clearance K791676 for PERITONEAL DIALYSIS CYCLER MODEL PDC1000, Substantially Equivalent on 1979-12-06. Applicant: J.M. Sounds Electronics Co.. Device class: 2.

Clearance details

Applicant: J.M. Sounds Electronics Co.
Product code: Code KPF
Device class: Class 2
Regulation: 21 CFR 876.5630
Advisory panel: Gastroenterology, Urology
Date received: 1979-08-27
Decision date: 1979-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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