WAVESCAN WAVEFRONT SYSTEM MODEL HS 1— 510(k) K000327

Unknown

Visx, Incorporated

FDA 510(k) clearance K000327 for WAVESCAN WAVEFRONT SYSTEM MODEL HS 1, Unknown on 2000-05-02. Applicant: Visx, Incorporated. Device class: 1.

Clearance details

Applicant: Visx, Incorporated
Product code: Code HKO
Device class: Class 1
Regulation: 21 CFR 886.1760
Advisory panel: Ophthalmic
Date received: 2000-02-02
Decision date: 2000-05-02
Decision: Unknown
Clearance type: Traditional
Location: Santa Ana, 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.