FDA 510(k)

Passio Pump Drainage System

K-Number: K230319 · 2023-11-24

Decision Date2023-11-24

Product CodePNG

Advisory CommitteeGU

DecisionUnknown

Device Summary

Passio Pump Drainage System is a medical device manufactured by Bearpac Medical. It received FDA 510(k) clearance on 2023-11-24 under approval number K230319. The device is classified under product code PNG. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the Passio Pump Drainage System?

Passio Pump Drainage System is a medical device that received FDA 510(k) clearance on 2023-11-24. It is manufactured by Bearpac Medical. The 510(k) number is K230319.

When was Passio Pump Drainage System approved by the FDA?

Passio Pump Drainage System received FDA 510(k) clearance on 2023-11-24, under approval number K230319.

What company makes Passio Pump Drainage System?

Passio Pump Drainage System is manufactured by Bearpac Medical.

What is the FDA product code for Passio Pump Drainage System?

The FDA product code for Passio Pump Drainage System is PNG.

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Other Devices by Bearpac Medical

K190292Passio Pump Drainage System K201404Passio Pump Drainage System

Related Devices (Code: PNG)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.