PILAIRO NASAL PILLOWS MASK
K-Number: K120027 · 2012-02-23
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Device Summary
Frequently Asked Questions
What is the PILAIRO NASAL PILLOWS MASK?
PILAIRO NASAL PILLOWS MASK is a medical device that received FDA 510(k) clearance on 2012-02-23. The listed applicant is Fisher & Paykel Healthcare Limited. The 510(k) number is K120027.
When did PILAIRO NASAL PILLOWS MASK receive FDA 510(k) clearance?
PILAIRO NASAL PILLOWS MASK received FDA 510(k) clearance on 2012-02-23, under 510(k) number K120027.
Who is the listed applicant for PILAIRO NASAL PILLOWS MASK?
The FDA 510(k) record lists Fisher & Paykel Healthcare Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PILAIRO NASAL PILLOWS MASK?
The FDA product code for PILAIRO NASAL PILLOWS 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 Limited 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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