KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5— 510(k) K870203

Name: FDA 510(k) clearance K870203
Creator: U.S. Food and Drug Administration
Published: 1987-02-12

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K870203 for KEELER LVA SYSTEM MULTI-CAP SERIES LVA51-1/2/3/4/5, Substantially Equivalent on 1987-02-12. Applicant: Keeler Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HKK
Device class: Class 1
Regulation: 21 CFR 886.5870
Advisory panel: Ophthalmic
Date received: 1987-01-20
Decision date: 1987-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

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