CANON AUTO REF KERATOMETER RK-1
FDA 510(k) clearance K861415 · decided 1986-05-14
Clearance details
- K-number
- K861415
- Device name
- CANON AUTO REF KERATOMETER RK-1
- Applicant
- Canon USA, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-04-15
- Decision date
- 1986-05-14
- Days to decision
- 29 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Jericho, NY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.