PERIDIAL PERITONEAL DIALYSIS TRAY— 510(k) K792207

Name: FDA 510(k) clearance K792207
Creator: U.S. Food and Drug Administration
Published: 1979-12-10

Substantially Equivalent

Cutter Laboratories, Inc.

FDA 510(k) clearance K792207 for PERIDIAL PERITONEAL DIALYSIS TRAY, Substantially Equivalent on 1979-12-10. Applicant: Cutter Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Cutter Laboratories, Inc.
Product code: Code FKG
Device class: Class 1
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1979-11-02
Decision date: 1979-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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