ELECTRORETINOGRAPH— 510(k) K760199

Substantially Equivalent

Lkc Technologies, Inc.

FDA 510(k) clearance K760199 for ELECTRORETINOGRAPH, Substantially Equivalent on 1976-08-04. Applicant: Lkc Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Lkc Technologies, Inc.
Product code: Code HLZ
Device class: Class 2
Regulation: 21 CFR 886.1220
Advisory panel: Ophthalmic
Date received: 1976-07-07
Decision date: 1976-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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