DeviceClearance

KEELER PULSAIR NON CONTACT TONOMETER, MODIFICATION— 510(k) K911721

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K911721 for KEELER PULSAIR NON CONTACT TONOMETER, MODIFICATION, Substantially Equivalent on 1991-06-25. Applicant: Keeler Instruments, Inc..

Clearance details

Applicant
Keeler Instruments, Inc.
Product code
Code HKX
Advisory panel
Ophthalmic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Broomall, PA, US
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