KEELER DUAL LIGHTSOURCE— 510(k) K861746

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K861746 for KEELER DUAL LIGHTSOURCE, Substantially Equivalent on 1986-08-21. Applicant: Keeler Instruments, Inc..

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HPQ
Advisory panel: Ophthalmic
Date received: 1986-05-06
Decision date: 1986-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.