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FDA 510(k)

AG-CLASSIC

K-Number: K072494 · 2008-02-12

ApplicantMedel S.P.A.
Decision Date2008-02-12
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AG-CLASSIC is the device name listed in this FDA 510(k) record. The listed applicant is Medel S.P.A.. It received FDA 510(k) clearance on 2008-02-12 under 510(k) number K072494. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AG-CLASSIC?

AG-CLASSIC is a medical device that received FDA 510(k) clearance on 2008-02-12. The listed applicant is Medel S.P.A.. The 510(k) number is K072494.

When did AG-CLASSIC receive FDA 510(k) clearance?

AG-CLASSIC received FDA 510(k) clearance on 2008-02-12, under 510(k) number K072494.

Who is the listed applicant for AG-CLASSIC?

The FDA 510(k) record lists Medel S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AG-CLASSIC?

The FDA product code for AG-CLASSIC is CAF.

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Other records listing Medel S.P.A. as applicant

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Related Devices (Code: CAF)

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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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