CORNEASCOPE MODEL 1200— 510(k) K850665

Substantially Equivalent

Kera Corp.

FDA 510(k) clearance K850665 for CORNEASCOPE MODEL 1200, Substantially Equivalent on 1985-03-20. Applicant: Kera Corp.. Device class: 1.

Clearance details

Applicant: Kera Corp.
Product code: Code HLQ
Device class: Class 1
Regulation: 21 CFR 886.1350
Advisory panel: Ophthalmic
Date received: 1985-02-20
Decision date: 1985-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.