THE MONITOR ELECTRONIC BED ALARM SYSTEM
K-Number: K901330 · 1990-08-30
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Device Summary
Frequently Asked Questions
What is the THE MONITOR ELECTRONIC BED ALARM SYSTEM?
THE MONITOR ELECTRONIC BED ALARM SYSTEM is a medical device that received FDA 510(k) clearance on 1990-08-30. The listed applicant is The Monitor Corp.. The 510(k) number is K901330.
When did THE MONITOR ELECTRONIC BED ALARM SYSTEM receive FDA 510(k) clearance?
THE MONITOR ELECTRONIC BED ALARM SYSTEM received FDA 510(k) clearance on 1990-08-30, under 510(k) number K901330.
Who is the listed applicant for THE MONITOR ELECTRONIC BED ALARM SYSTEM?
The FDA 510(k) record lists The Monitor Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE MONITOR ELECTRONIC BED ALARM SYSTEM?
The FDA product code for THE MONITOR ELECTRONIC BED ALARM SYSTEM is KMI.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KMI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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