MAINSTER RETINA LASER LENS— 510(k) K863911
Substantially EquivalentOcular Instruments, Inc.
FDA 510(k) clearance K863911 for MAINSTER RETINA LASER LENS, Substantially Equivalent on 1986-12-12. Applicant: Ocular Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Ocular Instruments, Inc.
- Product code
- Code HJK
- Device class
- Class 2
- Regulation
- 21 CFR 886.1385
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bellevue, WA, US
Recent devices under product code HJK
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