SLEEPSENSE SLEEP SENSORS
K-Number: K042253 · 2004-10-06
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Device Summary
Frequently Asked Questions
What is the SLEEPSENSE SLEEP SENSORS?
SLEEPSENSE SLEEP SENSORS is a medical device that received FDA 510(k) clearance on 2004-10-06. The listed applicant is S.L.P. , Ltd.. The 510(k) number is K042253.
When did SLEEPSENSE SLEEP SENSORS receive FDA 510(k) clearance?
SLEEPSENSE SLEEP SENSORS received FDA 510(k) clearance on 2004-10-06, under 510(k) number K042253.
Who is the listed applicant for SLEEPSENSE SLEEP SENSORS?
The FDA 510(k) record lists S.L.P. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SLEEPSENSE SLEEP SENSORS?
The FDA product code for SLEEPSENSE SLEEP SENSORS is MNR.
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 S.L.P. , Ltd. 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: MNR)
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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