VIEWPOINT CK SYSTEM
FDA premarket approval P010018/S008 · decided 2005-09-30
Approval details
- PMA number
- P010018
- Supplement
- S008
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VIEWPOINT CK SYSTEM
- Generic name
- Electrosurgical, radio frequency, refractive correction
- Applicant
- Refractec, Inc.
- Date received
- 2005-09-08
- Decision date
- 2005-09-30
- Days to decision
- 22 days
- Decision code
- OK30
- Product code
- MWD
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Irvine, CA
- Statement
- IMPLEMENTATION OF A CONTROLLED ADHESIVE APPLICATION PROCESS TO MORE ACCURATELY CONTROL THE AMOUNT OF ADHESIVE APPLIED.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| OPTIPOINT CORNEAL MARKER, MODEL VPT-OPT-450 (K053475) | Refractec, Inc. | 2006-03-03 |
| REFRACTEC MCS-100 (K980522) | Refractec, Inc. | 1998-07-22 |