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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 the device name listed in this FDA 510(k) record. The listed applicant is Ga Health Company Limited. It received FDA 510(k) clearance on 2023-08-01 under 510(k) 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. The listed applicant is Ga Health Company Limited. The 510(k) number is K231602.

When did Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing receive FDA 510(k) clearance?

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

Who is the listed applicant for Protego Air Water Connector; Protego Air Water Bottle Tubing; Protego Hybrid Tubing?

The FDA 510(k) record lists Ga Health Company Limited as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Ga Health Company Limited as applicant

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Related Devices (Code: OCX)

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.

K251986AUXILIARY WATER TUBE MAJ-855Olympus Medical Systems CorporationK251997Single-Use Biopsy Valve (MAJ-1555)Olympus Medical Systems CorporationK242586ArgoCap (200.52)Ovesco Endoscopy AGK241704Endoscopic Water PumpHangzhou AGS MedTech Co., Ltd.K242357Water Container (MAJ-901); Water Container (MAJ-902)Olympus Medical Systems CorporationK241874Aspiration Catheter (2189)Hobbs Medical, Inc.

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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