BED ALERT
K-Number: K872522 · 1988-01-19
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Device Summary
Frequently Asked Questions
What is the BED ALERT?
BED ALERT is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Nite Train-R Enterprises, Inc.. The 510(k) number is K872522.
When did BED ALERT receive FDA 510(k) clearance?
BED ALERT received FDA 510(k) clearance on 1988-01-19, under 510(k) number K872522.
Who is the listed applicant for BED ALERT?
The FDA 510(k) record lists Nite Train-R Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BED ALERT?
The FDA product code for BED ALERT is KPN.
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.
Other records listing Nite Train-R Enterprises, Inc. as applicant
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: KPN)
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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