EOL, MODEL LIO— 510(k) K881984

Substantially Equivalent

Eol, Inc.

FDA 510(k) clearance K881984 for EOL, MODEL LIO, Substantially Equivalent on 1988-09-06. Applicant: Eol, Inc.. Device class: 2.

Clearance details

Applicant: Eol, Inc.
Product code: Code HLI
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1988-05-12
Decision date: 1988-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oak Ridge, TN, US

Download summary PDF View on FDA.gov ↗

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