NIDEK KM-800 AUTO KERATOMETER— 510(k) K861063

Substantially Equivalent

Nidek, Inc.

FDA 510(k) clearance K861063 for NIDEK KM-800 AUTO KERATOMETER, Substantially Equivalent on 1986-04-04. Applicant: Nidek, Inc..

Clearance details

Applicant: Nidek, Inc.
Product code: Code HLQ
Advisory panel: Ophthalmic
Date received: 1986-03-20
Decision date: 1986-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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