REPROCESSED PHACOEMULSIFICATION TIPS— 510(k) K060648

Name: FDA 510(k) clearance K060648
Creator: U.S. Food and Drug Administration
Published: 2007-03-19

Substantially Equivalent

Alliance Medical Corp.

FDA 510(k) clearance K060648 for REPROCESSED PHACOEMULSIFICATION TIPS, Substantially Equivalent on 2007-03-19. Applicant: Alliance Medical Corp.. Device class: 2.

Clearance details

Applicant: Alliance Medical Corp.
Product code: Code NKX
Device class: Class 2
Regulation: 21 CFR 886.4670
Advisory panel: Ophthalmic
Date received: 2006-03-13
Decision date: 2007-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, 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.