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FDA 510(k)

AEQUOS

K-Number: K033260 · 2004-12-07

ApplicantAap Implantate AG
Decision Date2004-12-07
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AEQUOS is the device name listed in this FDA 510(k) record. The listed applicant is Aap Implantate AG. It received FDA 510(k) clearance on 2004-12-07 under 510(k) number K033260. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEQUOS?

AEQUOS is a medical device that received FDA 510(k) clearance on 2004-12-07. The listed applicant is Aap Implantate AG. The 510(k) number is K033260.

When did AEQUOS receive FDA 510(k) clearance?

AEQUOS received FDA 510(k) clearance on 2004-12-07, under 510(k) number K033260.

Who is the listed applicant for AEQUOS?

The FDA 510(k) record lists Aap Implantate AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AEQUOS?

The FDA product code for AEQUOS is JWH.

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Related Devices (Code: JWH)

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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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