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FDA 510(k)

ADVENTURE A10

K-Number: K042535 · 2004-10-05

ApplicantUlrich Alber GmbH
Decision Date2004-10-05
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ADVENTURE A10 is the device name listed in this FDA 510(k) record. The listed applicant is Ulrich Alber GmbH. It received FDA 510(k) clearance on 2004-10-05 under 510(k) number K042535. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVENTURE A10?

ADVENTURE A10 is a medical device that received FDA 510(k) clearance on 2004-10-05. The listed applicant is Ulrich Alber GmbH. The 510(k) number is K042535.

When did ADVENTURE A10 receive FDA 510(k) clearance?

ADVENTURE A10 received FDA 510(k) clearance on 2004-10-05, under 510(k) number K042535.

Who is the listed applicant for ADVENTURE A10?

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

What is the FDA product code for ADVENTURE A10?

The FDA product code for ADVENTURE A10 is ITI.

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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.

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