LCA 2000— 510(k) K871034

Substantially Equivalent

Vistek Corp.

FDA 510(k) clearance K871034 for LCA 2000, Substantially Equivalent on 1987-04-10. Applicant: Vistek Corp.. Device class: 2.

Clearance details

Applicant
Vistek Corp.
Product code
Code FTA
Device class
Class 2
Regulation
21 CFR 878.4580
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Santa Barbara, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.