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FDA 510(k)

Mais Central Venous Catheter

K-Number: K221827 · 2023-06-23

ApplicantSaudi Mais Co. For Medical Products
Decision Date2023-06-23
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Mais Central Venous Catheter is a medical device manufactured by Saudi Mais Co. For Medical Products. It received FDA 510(k) clearance on 2023-06-23 under approval number K221827. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mais Central Venous Catheter?

Mais Central Venous Catheter is a medical device that received FDA 510(k) clearance on 2023-06-23. It is manufactured by Saudi Mais Co. For Medical Products. The 510(k) number is K221827.

When was Mais Central Venous Catheter approved by the FDA?

Mais Central Venous Catheter received FDA 510(k) clearance on 2023-06-23, under approval number K221827.

What company makes Mais Central Venous Catheter?

Mais Central Venous Catheter is manufactured by Saudi Mais Co. For Medical Products.

What is the FDA product code for Mais Central Venous Catheter?

The FDA product code for Mais Central Venous Catheter is FOZ.

Related Clinical Trials

NCT07612683 Pulmonary Artery Catheters in Cardiac Surgery NOT_YET_RECRUITING NCT07610681 Midline Catheter Study ACTIVE_NOT_RECRUITING NCT07095660 RECANA OUS - Recana Thrombectomy Catheter System for Venous Obstruction and Occlusion Study (RECANA-OUS-IRL) RECRUITING NCT06472518 Pharmaco Mechanical Thrombolysis Associated With Anticoagulation Compared With Anticoagulation in the Acute Phase of Very Symptomatic Proximal Venous Thrombosis of the Lower Limbs. RECRUITING NCT07587593 The IVCare Adaptive Platform Trial NOT_YET_RECRUITING NCT07585188 Neonatal Catheter Lock for Infection Prevention NOT_YET_RECRUITING

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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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