Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SLEEPWEAVER ELAN NASAL CPAP MASK

K-Number: K120757 · 2012-04-24

Decision Date2012-04-24
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SLEEPWEAVER ELAN NASAL CPAP MASK is the device name listed in this FDA 510(k) record. The listed applicant is Circadiance, LLC. It received FDA 510(k) clearance on 2012-04-24 under 510(k) number K120757. 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 SLEEPWEAVER ELAN NASAL CPAP MASK?

SLEEPWEAVER ELAN NASAL CPAP MASK is a medical device that received FDA 510(k) clearance on 2012-04-24. The listed applicant is Circadiance, LLC. The 510(k) number is K120757.

When did SLEEPWEAVER ELAN NASAL CPAP MASK receive FDA 510(k) clearance?

SLEEPWEAVER ELAN NASAL CPAP MASK received FDA 510(k) clearance on 2012-04-24, under 510(k) number K120757.

Who is the listed applicant for SLEEPWEAVER ELAN NASAL CPAP MASK?

The FDA 510(k) record lists Circadiance, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLEEPWEAVER ELAN NASAL CPAP MASK?

The FDA product code for SLEEPWEAVER ELAN NASAL CPAP MASK 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 Circadiance, LLC 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.

↑