CANON AUTO KERATOMETER K-1— 510(k) K844054
Substantially EquivalentCanon USA, Inc.
FDA 510(k) clearance K844054 for CANON AUTO KERATOMETER K-1, Substantially Equivalent on 1984-12-19. Applicant: Canon USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Canon USA, Inc.
- Product code
- Code HLI
- Device class
- Class 2
- Regulation
- 21 CFR 886.1570
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Success, NY, US
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