REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM
K-Number: K090243 · 2009-05-08
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Device Summary
Frequently Asked Questions
What is the REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM?
REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM is a medical device that received FDA 510(k) clearance on 2009-05-08. The listed applicant is Respironics Inc., Sleep & Home Respiratory Group. The 510(k) number is K090243.
When did REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM receive FDA 510(k) clearance?
REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM received FDA 510(k) clearance on 2009-05-08, under 510(k) number K090243.
Who is the listed applicant for REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM?
The FDA 510(k) record lists Respironics Inc., Sleep & Home Respiratory Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM?
The FDA product code for REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM 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., Sleep & Home Respiratory Group 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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