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FDA 510(k)

REMSTAR AFLEX CPAP SYSTEM

K-Number: K063830 · 2007-03-09

Decision Date2007-03-09
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REMSTAR AFLEX CPAP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Respironics Inc., Sleep & Home Respiratory Group. It received FDA 510(k) clearance on 2007-03-09 under 510(k) number K063830. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REMSTAR AFLEX CPAP SYSTEM?

REMSTAR AFLEX CPAP SYSTEM is a medical device that received FDA 510(k) clearance on 2007-03-09. The listed applicant is Respironics Inc., Sleep & Home Respiratory Group. The 510(k) number is K063830.

When did REMSTAR AFLEX CPAP SYSTEM receive FDA 510(k) clearance?

REMSTAR AFLEX CPAP SYSTEM received FDA 510(k) clearance on 2007-03-09, under 510(k) number K063830.

Who is the listed applicant for REMSTAR 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 AFLEX CPAP SYSTEM?

The FDA product code for REMSTAR 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.

View all 21 devices →

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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