ALERT BED ALARM SYSTEM— 510(k) K901969

Substantially Equivalent

Alertronics, Inc.

FDA 510(k) clearance K901969 for ALERT BED ALARM SYSTEM, Substantially Equivalent on 1990-09-12. Applicant: Alertronics, Inc.. Device class: 1.

Clearance details

Applicant: Alertronics, Inc.
Product code: Code KMI
Device class: Class 1
Regulation: 21 CFR 880.2400
Advisory panel: General Hospital
Date received: 1990-05-01
Decision date: 1990-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tulsa, OK, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.