FDA 510(k)

PNEUMOCLEAR

K-Number: K170784 · 2017-05-15

Decision Date2017-05-15

Product CodeHIF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

PNEUMOCLEAR is a medical device manufactured by W.O.M. World of Medicine GmbH. It received FDA 510(k) clearance on 2017-05-15 under approval number K170784. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PNEUMOCLEAR?

PNEUMOCLEAR is a medical device that received FDA 510(k) clearance on 2017-05-15. It is manufactured by W.O.M. World of Medicine GmbH. The 510(k) number is K170784.

When was PNEUMOCLEAR approved by the FDA?

PNEUMOCLEAR received FDA 510(k) clearance on 2017-05-15, under approval number K170784.

What company makes PNEUMOCLEAR?

PNEUMOCLEAR is manufactured by W.O.M. World of Medicine GmbH.

What is the FDA product code for PNEUMOCLEAR?

The FDA product code for PNEUMOCLEAR is HIF.

Other Devices by W.O.M. World of Medicine GmbH

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Related Devices (Code: HIF)

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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.