F&P Optiflow Flow Diverter— 510(k) K234053
Substantially EquivalentFisher & Paykel Healthcare, Ltd.
FDA 510(k) clearance K234053 for F&P Optiflow Flow Diverter, Substantially Equivalent on 2024-08-09. Applicant: Fisher & Paykel Healthcare, Ltd.. Device class: 2.
Clearance details
- Applicant
- Fisher & Paykel Healthcare, Ltd.
- Product code
- Code CBP
- Device class
- Class 2
- Regulation
- 21 CFR 868.5870
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Auckland, NZ
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Data sourced from openFDA. This site is unofficial and independent of the FDA.