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FDA 510(k)

ADDPLUS

K-Number: K090841 · 2009-10-05

ApplicantUlrich GmbH & Co. KG
Decision Date2009-10-05
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ADDPLUS 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 2009-10-05 under 510(k) number K090841. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADDPLUS?

ADDPLUS is a medical device that received FDA 510(k) clearance on 2009-10-05. The listed applicant is Ulrich GmbH & Co. KG. The 510(k) number is K090841.

When did ADDPLUS receive FDA 510(k) clearance?

ADDPLUS received FDA 510(k) clearance on 2009-10-05, under 510(k) number K090841.

Who is the listed applicant for ADDPLUS?

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 ADDPLUS?

The FDA product code for ADDPLUS is MQP.

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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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