DISETRONIC DOLOMAT PUMP— 510(k) K920063

Name: FDA 510(k) clearance K920063
Creator: U.S. Food and Drug Administration
Published: 1993-08-03

Substantially Equivalent

Disetronic Medical Systems

FDA 510(k) clearance K920063 for DISETRONIC DOLOMAT PUMP, Substantially Equivalent on 1993-08-03. Applicant: Disetronic Medical Systems. Device class: 1.

Clearance details

Applicant: Disetronic Medical Systems
Product code: Code FRW
Device class: Class 1
Regulation: 21 CFR 880.2720
Advisory panel: General Hospital
Date received: 1992-01-07
Decision date: 1993-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minnetonka, MN, US

Download summary PDF View on FDA.gov ↗

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