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FDA 510(k)

ulrich Transfer Set

K-Number: K161723 · 2016-12-21

Decision Date2016-12-21
Product CodePQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ulrich Transfer Set is a medical device manufactured by Ulrich GmbH & Co. KG. It received FDA 510(k) clearance on 2016-12-21 under approval number K161723. The device is classified under product code PQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ulrich Transfer Set?

ulrich Transfer Set is a medical device that received FDA 510(k) clearance on 2016-12-21. It is manufactured by Ulrich GmbH & Co. KG. The 510(k) number is K161723.

When was ulrich Transfer Set approved by the FDA?

ulrich Transfer Set received FDA 510(k) clearance on 2016-12-21, under approval number K161723.

What company makes ulrich Transfer Set?

ulrich Transfer Set is manufactured by Ulrich GmbH & Co. KG.

What is the FDA product code for ulrich Transfer Set?

The FDA product code for ulrich Transfer Set is PQH.

Other Devices by Ulrich GmbH & Co. KG

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Related Devices (Code: PQH)

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.