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 the device name listed in this FDA 510(k) record. The listed applicant is Ulrich GmbH & Co. KG. It received FDA 510(k) clearance on 2016-12-21 under 510(k) 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. The listed applicant is Ulrich GmbH & Co. KG. The 510(k) number is K161723.

When did ulrich Transfer Set receive FDA 510(k) clearance?

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

Who is the listed applicant for ulrich Transfer Set?

The FDA 510(k) record lists Ulrich GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ulrich Transfer Set?

The FDA product code for ulrich Transfer Set is PQH.

Other records listing Ulrich GmbH & Co. KG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.