FDA 510(k)

Voyant 5mm Fusion Device, Voyant Maryland Fusion Device

Numéro K : K193292 · 2019-12-20

DemandeurApplied Medical Resources Corp.

Date de décision2019-12-20

Code produitGEI

Comité consultatifSU

DécisionSubstantially Equivalent

Résumé du dispositif

Voyant 5mm Fusion Device, Voyant Maryland Fusion Device is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources Corp.. It received FDA 510(k) clearance on 2019-12-20 under 510(k) number K193292. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Voyant 5mm Fusion Device, Voyant Maryland Fusion Device?

Voyant 5mm Fusion Device, Voyant Maryland Fusion Device is a medical device that received FDA 510(k) clearance on 2019-12-20. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K193292.

When did Voyant 5mm Fusion Device, Voyant Maryland Fusion Device receive FDA 510(k) clearance?

Voyant 5mm Fusion Device, Voyant Maryland Fusion Device received FDA 510(k) clearance on 2019-12-20, under 510(k) number K193292.

Who is the listed applicant for Voyant 5mm Fusion Device, Voyant Maryland Fusion Device?

The FDA 510(k) record lists Applied Medical Resources Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Voyant 5mm Fusion Device, Voyant Maryland Fusion Device?

The FDA product code for Voyant 5mm Fusion Device, Voyant Maryland Fusion Device is GEI.

Essais cliniques associés

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Source officielle

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