HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER— 510(k) K891610
Substantially EquivalentKeeler Instruments, Inc.
FDA 510(k) clearance K891610 for HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER, Substantially Equivalent on 1989-06-05. Applicant: Keeler Instruments, Inc.. Device class: 1.
Clearance details
- Applicant
- Keeler Instruments, Inc.
- Product code
- Code HOD
- Device class
- Class 1
- Regulation
- 21 CFR 886.4350
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Broomall, PA, US
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