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FDA 510(k)

INTERWORKS

K-Number: K070755 · 2007-05-08

ApplicantAvreo, Inc.
Decision Date2007-05-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERWORKS is the device name listed in this FDA 510(k) record. The listed applicant is Avreo, Inc.. It received FDA 510(k) clearance on 2007-05-08 under 510(k) number K070755. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERWORKS?

INTERWORKS is a medical device that received FDA 510(k) clearance on 2007-05-08. The listed applicant is Avreo, Inc.. The 510(k) number is K070755.

When did INTERWORKS receive FDA 510(k) clearance?

INTERWORKS received FDA 510(k) clearance on 2007-05-08, under 510(k) number K070755.

Who is the listed applicant for INTERWORKS?

The FDA 510(k) record lists Avreo, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERWORKS?

The FDA product code for INTERWORKS is LLZ.

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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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