MEDIC LUX DIAGNOSTIC SETS— 510(k) K832437

Name: FDA 510(k) clearance K832437
Creator: U.S. Food and Drug Administration
Published: 1983-08-16

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K832437 for MEDIC LUX DIAGNOSTIC SETS, Substantially Equivalent on 1983-08-16. Applicant: Keeler Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HLJ
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1983-07-25
Decision date: 1983-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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