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FDA 510(k)

Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing

K-Number: K231602 · 2023-08-01

ApplicantGa Health Company Limited
Decision Date2023-08-01
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing is a medical device manufactured by Ga Health Company Limited. It received FDA 510(k) clearance on 2023-08-01 under approval number K231602. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing?

Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing is a medical device that received FDA 510(k) clearance on 2023-08-01. It is manufactured by Ga Health Company Limited. The 510(k) number is K231602.

When was Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing approved by the FDA?

Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing received FDA 510(k) clearance on 2023-08-01, under approval number K231602.

What company makes Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing?

Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing is manufactured by Ga Health Company Limited.

What is the FDA product code for Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing?

The FDA product code for Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing is OCX.

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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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