VISTAKON (ETAFILICON A) ACUVUE(R),SUREVUE(R) LENS
FDA premarket approval N18033/S027 · decided 1995-02-13
Approval details
- PMA number
- N18033
- Supplement
- S027
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VISTAKON (ETAFILICON A) ACUVUE(R),SUREVUE(R) LENS
- Generic name
- Lenses, soft contact, daily wear
- Applicant
- Vistakon, Johnson & Johnson Vision Products, Inc.
- Date received
- 1993-05-14
- Decision date
- 1995-02-13
- Days to decision
- 640 days
- Decision code
- APPR
- Product code
- LPL
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Jacksonville, FL
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