BED PATIENT PRESENCE MONITOR— 510(k) K871203

Name: FDA 510(k) clearance K871203
Creator: U.S. Food and Drug Administration
Published: 1987-05-26

Substantially Equivalent

Human Technologies, Inc.

FDA 510(k) clearance K871203 for BED PATIENT PRESENCE MONITOR, Substantially Equivalent on 1987-05-26. Applicant: Human Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Human Technologies, Inc.
Product code: Code KMI
Device class: Class 1
Regulation: 21 CFR 880.2400
Advisory panel: General Hospital
Date received: 1987-03-25
Decision date: 1987-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Petersburg, FL, US

Download summary PDF View on FDA.gov ↗

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