OSHER SURGICAL GONIO/POSTERIOR POLE LENS— 510(k) K935302
Substantially EquivalentOcular Instruments, Inc.
FDA 510(k) clearance K935302 for OSHER SURGICAL GONIO/POSTERIOR POLE LENS, Substantially Equivalent on 1994-04-01. Applicant: Ocular Instruments, Inc.. Device class: 1.
Clearance details
- Applicant
- Ocular Instruments, Inc.
- Product code
- Code HKS
- Device class
- Class 1
- Regulation
- 21 CFR 886.1660
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bellevue, WA, US
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