THE MONITOR ELECTRONIC BED ALARM SYSTEM— 510(k) K901330

Name: FDA 510(k) clearance K901330
Creator: U.S. Food and Drug Administration
Published: 1990-08-30

Substantially Equivalent

The Monitor Corp.

FDA 510(k) clearance K901330 for THE MONITOR ELECTRONIC BED ALARM SYSTEM, Substantially Equivalent on 1990-08-30. Applicant: The Monitor Corp.. Device class: 1.

Clearance details

Applicant: The Monitor Corp.
Product code: Code KMI
Device class: Class 1
Regulation: 21 CFR 880.2400
Advisory panel: General Hospital
Date received: 1990-03-22
Decision date: 1990-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, 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.