F&P 950 Accessory Breathing Circuit Kits
K-Number: K221436 · 2023-06-29
Device Summary
Frequently Asked Questions
What is the F&P 950 Accessory Breathing Circuit Kits?
F&P 950 Accessory Breathing Circuit Kits is a medical device that received FDA 510(k) clearance on 2023-06-29. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K221436.
When did F&P 950 Accessory Breathing Circuit Kits receive FDA 510(k) clearance?
F&P 950 Accessory Breathing Circuit Kits received FDA 510(k) clearance on 2023-06-29, under 510(k) number K221436.
Who is the listed applicant for F&P 950 Accessory Breathing Circuit Kits?
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 F&P 950 Accessory Breathing Circuit Kits?
The FDA product code for F&P 950 Accessory Breathing Circuit Kits is BZD.
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.