KERATO ANALYZER (EKA)— 510(k) K040373

Substantially Equivalent

Konan Medical, Inc.

FDA 510(k) clearance K040373 for KERATO ANALYZER (EKA), Substantially Equivalent on 2004-03-19. Applicant: Konan Medical, Inc.. Device class: 2.

Clearance details

Applicant: Konan Medical, Inc.
Product code: Code NQE
Device class: Class 2
Regulation: 21 CFR 886.1850
Advisory panel: Ophthalmic
Date received: 2004-02-17
Decision date: 2004-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hasbrouck Heights, NJ, US

Download summary PDF View on FDA.gov ↗

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