KEELER FIBEROPTIC HEADLAMP— 510(k) K861747

Name: FDA 510(k) clearance K861747
Creator: U.S. Food and Drug Administration
Published: 1986-08-21

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K861747 for KEELER FIBEROPTIC HEADLAMP, Substantially Equivalent on 1986-08-21. Applicant: Keeler Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HPQ
Device class: Class 2
Regulation: 21 CFR 886.4335
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 ↗

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K861746 — KEELER DUAL LIGHTSOURCE1986-08-21
K822272 — HEAD MIRRORS W/HEAD LAMPS & HEAD BANDS1982-11-10

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