M-SERIES PRO CPAP SYTEM
K-Number: K052110 · 2005-10-20
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Device Summary
Frequently Asked Questions
What is the M-SERIES PRO CPAP SYTEM?
M-SERIES PRO CPAP SYTEM is a medical device that received FDA 510(k) clearance on 2005-10-20. The listed applicant is Respironics, Inc.. The 510(k) number is K052110.
When did M-SERIES PRO CPAP SYTEM receive FDA 510(k) clearance?
M-SERIES PRO CPAP SYTEM received FDA 510(k) clearance on 2005-10-20, under 510(k) number K052110.
Who is the listed applicant for M-SERIES PRO CPAP SYTEM?
The FDA 510(k) record lists Respironics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for M-SERIES PRO CPAP SYTEM?
The FDA product code for M-SERIES PRO CPAP SYTEM 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.
Other records listing Respironics, 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: 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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