FDA 510(k), K182902, Precision1
FDA 510(k), K182902, Precision1
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$149.00 USD
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510(K) Number: K182902
Device Name: Precision1
Manufacturer: Alicia Plesnarski
Device Classification Name: Lenses, Soft Contact, Daily Wear
Regulation Number: LPL
Classification Product Code: 10/16/2018
Date Received: 12/11/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ophthalmic
Device Name: Precision1
Manufacturer: Alicia Plesnarski
Device Classification Name: Lenses, Soft Contact, Daily Wear
Regulation Number: LPL
Classification Product Code: 10/16/2018
Date Received: 12/11/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ophthalmic