ZEST NASAL MASK
K-Number: K083832 · 2009-03-16
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Device Summary
Frequently Asked Questions
What is the ZEST NASAL MASK?
ZEST NASAL MASK is a medical device that received FDA 510(k) clearance on 2009-03-16. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K083832.
When did ZEST NASAL MASK receive FDA 510(k) clearance?
ZEST NASAL MASK received FDA 510(k) clearance on 2009-03-16, under 510(k) number K083832.
Who is the listed applicant for ZEST NASAL MASK?
The FDA 510(k) record lists Fisher & Paykel Healthcare, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZEST NASAL MASK?
The FDA product code for ZEST NASAL 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 Fisher & Paykel Healthcare, Ltd. 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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