BED PATIENT MONITOR— 510(k) K854950

Name: FDA 510(k) clearance K854950
Creator: U.S. Food and Drug Administration
Published: 1986-03-25

Substantially Equivalent

Clearview Electronics Corp.

FDA 510(k) clearance K854950 for BED PATIENT MONITOR, Substantially Equivalent on 1986-03-25. Applicant: Clearview Electronics Corp.. Device class: 1.

Clearance details

Applicant: Clearview Electronics Corp.
Product code: Code KMI
Device class: Class 1
Regulation: 21 CFR 880.2400
Advisory panel: General Hospital
Date received: 1985-12-10
Decision date: 1986-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newark, DE, 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.