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FDA 510(k)

F&P 950 Accessory Breathing Circuit Kits

K-Number: K221436 · 2023-06-29

ApplicantFisher & Paykel Healthcare, Ltd.
Decision Date2023-06-29
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

F&P 950 Accessory Breathing Circuit Kits is a medical device manufactured by Fisher & Paykel Healthcare, Ltd.. It received FDA 510(k) clearance on 2023-06-29 under approval number K221436. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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. It is manufactured by Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K221436.

When was F&P 950 Accessory Breathing Circuit Kits approved by the FDA?

F&P 950 Accessory Breathing Circuit Kits received FDA 510(k) clearance on 2023-06-29, under approval number K221436.

What company makes F&P 950 Accessory Breathing Circuit Kits?

F&P 950 Accessory Breathing Circuit Kits is manufactured by Fisher & Paykel Healthcare, Ltd..

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.

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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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