FLEXIFIT HC432 FULL FACE MASK
K-Number: K061236 · 2006-08-29
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Device Summary
Frequently Asked Questions
What is the FLEXIFIT HC432 FULL FACE MASK?
FLEXIFIT HC432 FULL FACE MASK is a medical device that received FDA 510(k) clearance on 2006-08-29. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K061236.
When did FLEXIFIT HC432 FULL FACE MASK receive FDA 510(k) clearance?
FLEXIFIT HC432 FULL FACE MASK received FDA 510(k) clearance on 2006-08-29, under 510(k) number K061236.
Who is the listed applicant for FLEXIFIT HC432 FULL FACE 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 FLEXIFIT HC432 FULL FACE MASK?
The FDA product code for FLEXIFIT HC432 FULL FACE 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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