FDA 510(k)

Recovery Pump, 737R (RPX)

K-Number: K190493 · 2019-05-15

Decision Date2019-05-15

Product CodeIRP

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Recovery Pump, 737R (RPX) is a medical device manufactured by Mego Afek AC , Ltd.. It received FDA 510(k) clearance on 2019-05-15 under approval number K190493. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Recovery Pump, 737R (RPX)?

Recovery Pump, 737R (RPX) is a medical device that received FDA 510(k) clearance on 2019-05-15. It is manufactured by Mego Afek AC , Ltd.. The 510(k) number is K190493.

When was Recovery Pump, 737R (RPX) approved by the FDA?

Recovery Pump, 737R (RPX) received FDA 510(k) clearance on 2019-05-15, under approval number K190493.

What company makes Recovery Pump, 737R (RPX)?

Recovery Pump, 737R (RPX) is manufactured by Mego Afek AC , Ltd..

What is the FDA product code for Recovery Pump, 737R (RPX)?

The FDA product code for Recovery Pump, 737R (RPX) is IRP.

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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.