REMSTAR AUTO CPAP SYSTEM
K-Number: K012554 · 2002-01-29
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Device Summary
Frequently Asked Questions
What is the REMSTAR AUTO CPAP SYSTEM?
REMSTAR AUTO CPAP SYSTEM is a medical device that received FDA 510(k) clearance on 2002-01-29. The listed applicant is Respironics, Inc.. The 510(k) number is K012554.
When did REMSTAR AUTO CPAP SYSTEM receive FDA 510(k) clearance?
REMSTAR AUTO CPAP SYSTEM received FDA 510(k) clearance on 2002-01-29, under 510(k) number K012554.
Who is the listed applicant for REMSTAR AUTO CPAP SYSTEM?
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 REMSTAR AUTO CPAP SYSTEM?
The FDA product code for REMSTAR AUTO 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. 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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