PERITONEAL DIALYSIS SYSTEM— 510(k) K760724

Name: FDA 510(k) clearance K760724
Creator: U.S. Food and Drug Administration
Published: 1976-11-23

Substantially Equivalent

Physio-Control Corp.

FDA 510(k) clearance K760724 for PERITONEAL DIALYSIS SYSTEM, Substantially Equivalent on 1976-11-23. Applicant: Physio-Control Corp.. Device class: 1.

Clearance details

Applicant: Physio-Control Corp.
Product code: Code EKX
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 1976-09-27
Decision date: 1976-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.