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FDA 510(k)

UCENTUM

K-Number: K123717 · 2013-03-04

ApplicantUlrich GmbH & Co. KG
Decision Date2013-03-04
Product CodeNKB
Advisory CommitteeOR
DecisionUnknown

Device Summary

UCENTUM 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 2013-03-04 under 510(k) number K123717. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the UCENTUM?

UCENTUM is a medical device that received FDA 510(k) clearance on 2013-03-04. The listed applicant is Ulrich GmbH & Co. KG. The 510(k) number is K123717.

When did UCENTUM receive FDA 510(k) clearance?

UCENTUM received FDA 510(k) clearance on 2013-03-04, under 510(k) number K123717.

Who is the listed applicant for UCENTUM?

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 UCENTUM?

The FDA product code for UCENTUM is NKB.

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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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