KEELER FIBEROPTIC HEADLAMP— 510(k) K861747

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K861747 for KEELER FIBEROPTIC HEADLAMP, 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

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