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FDA 510(k)

AG-PLUS, MODEL 91210

K-Number: K060404 · 2006-06-22

ApplicantMedel S.P.A.
Decision Date2006-06-22
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AG-PLUS, MODEL 91210 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 2006-06-22 under 510(k) number K060404. 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-PLUS, MODEL 91210?

AG-PLUS, MODEL 91210 is a medical device that received FDA 510(k) clearance on 2006-06-22. The listed applicant is Medel S.P.A.. The 510(k) number is K060404.

When did AG-PLUS, MODEL 91210 receive FDA 510(k) clearance?

AG-PLUS, MODEL 91210 received FDA 510(k) clearance on 2006-06-22, under 510(k) number K060404.

Who is the listed applicant for AG-PLUS, MODEL 91210?

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-PLUS, MODEL 91210?

The FDA product code for AG-PLUS, MODEL 91210 is CAF.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: CAF)

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Official Source

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