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FDA 510(k), K180299, ACUVUE OASYS (senofilcon A) with Photochromic Additive
FDA 510(k), K180299, ACUVUE OASYS (senofilcon A) with Photochromic Additive
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510(K) Number: K180299
Device Name: ACUVUE OASYS (senofilcon A) with Photochromic Additive
Manufacturer: Johnson & Johnson Vision Care, Inc.
Device Classification Name: lenses, soft contact, daily wear
Regulation Number: 886.5925
Classification Product Code: LPL
Date Received: 02/02/2018
Decision Date: 04/10/2018
Regulation Medical Specialty: Ophthalmic
Device Name: ACUVUE OASYS (senofilcon A) with Photochromic Additive
Manufacturer: Johnson & Johnson Vision Care, Inc.
Device Classification Name: lenses, soft contact, daily wear
Regulation Number: 886.5925
Classification Product Code: LPL
Date Received: 02/02/2018
Decision Date: 04/10/2018
Regulation Medical Specialty: Ophthalmic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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