MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY
K-Number: K071069 · 2007-06-12
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Device Summary
Frequently Asked Questions
What is the MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY?
MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY is a medical device that received FDA 510(k) clearance on 2007-06-12. The listed applicant is Viasys Sleep Systems, LLC. The 510(k) number is K071069.
When did MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY receive FDA 510(k) clearance?
MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY received FDA 510(k) clearance on 2007-06-12, under 510(k) number K071069.
Who is the listed applicant for MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY?
The FDA 510(k) record lists Viasys Sleep Systems, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY?
The FDA product code for MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY is BZD.
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: BZD)
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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