MODIFICATION TO OPTIMUM GP (OXYGEN PERMEABLE) DAILY WEAR CONTACT LENSES
FDA 510(k) clearance K062548 · decided 2006-11-01
Clearance details
- K-number
- K062548
- Device name
- MODIFICATION TO OPTIMUM GP (OXYGEN PERMEABLE) DAILY WEAR CONTACT LENSES
- Applicant
- Contamac, Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2006-08-30
- Decision date
- 2006-11-01
- Days to decision
- 63 days
- Clearance type
- Special
- Product code
- HQD
- Device class
- 2
- Regulation number
- 886.5916
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Grand Junction, CO, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| IGEL 67 CONTACT LENS (P860009/S002) | Contamac, Ltd. | 1989-05-09 |
| IDEL 67 CONTACT LENS (P860009/S001) | Contamac, Ltd. | 1987-10-13 |