FDA 510(k)

Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere

Numéro K : K210436 · 2021-04-12

Date de décision2021-04-12

Code produitLPL

Comité consultatifOP

DécisionSubstantially Equivalent

Résumé du dispositif

Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories, Inc.. It received FDA 510(k) clearance on 2021-04-12 under 510(k) number K210436. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere?

Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere is a medical device that received FDA 510(k) clearance on 2021-04-12. The listed applicant is Alcon Laboratories, Inc.. The 510(k) number is K210436.

When did Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere receive FDA 510(k) clearance?

Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere received FDA 510(k) clearance on 2021-04-12, under 510(k) number K210436.

Who is the listed applicant for Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere?

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

What is the FDA product code for Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere?

The FDA product code for Total30, Total30 for Astigmatism, Total30 Multifocal, Total30 Multifocal Toric, Total30 Asphere is LPL.

Essais cliniques associés

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Dispositifs connexes (Code : LPL)

Source officielle

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