SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM
K-Number: K080321 · 2008-05-23
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Device Summary
Frequently Asked Questions
What is the SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM?
SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 2008-05-23. The listed applicant is Snap Laboratories, LLC. The 510(k) number is K080321.
When did SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM receive FDA 510(k) clearance?
SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM received FDA 510(k) clearance on 2008-05-23, under 510(k) number K080321.
Who is the listed applicant for SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM?
The FDA 510(k) record lists Snap Laboratories, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM?
The FDA product code for SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM is MNR.
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 Snap Laboratories, 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: MNR)
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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