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FDA 510(k)

LAP-Pump PP110

K-Number: K163320 · 2017-03-21

ApplicantW.O.M. World of Medicine GmbH
Decision Date2017-03-21
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAP-Pump PP110 is the device name listed in this FDA 510(k) record. The listed applicant is W.O.M. World of Medicine GmbH. It received FDA 510(k) clearance on 2017-03-21 under 510(k) number K163320. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAP-Pump PP110?

LAP-Pump PP110 is a medical device that received FDA 510(k) clearance on 2017-03-21. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K163320.

When did LAP-Pump PP110 receive FDA 510(k) clearance?

LAP-Pump PP110 received FDA 510(k) clearance on 2017-03-21, under 510(k) number K163320.

Who is the listed applicant for LAP-Pump PP110?

The FDA 510(k) record lists W.O.M. World of Medicine GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAP-Pump PP110?

The FDA product code for LAP-Pump PP110 is HET.

Other records listing W.O.M. World of Medicine GmbH as applicant

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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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