KEELER PULSAIR NON CONTACT TONOMETER, MODIFICATION— 510(k) K911721
Substantially EquivalentKeeler Instruments, Inc.
FDA 510(k) clearance K911721 for KEELER PULSAIR NON CONTACT TONOMETER, MODIFICATION, Substantially Equivalent on 1991-06-25. Applicant: Keeler Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Keeler Instruments, Inc.
- Product code
- Code HKX
- Device class
- Class 2
- Regulation
- 21 CFR 886.1930
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Broomall, PA, US
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