SOPROLIFE— 510(k) K092583

Substantially Equivalent

Sopro

FDA 510(k) clearance K092583 for SOPROLIFE, Substantially Equivalent on 2010-01-13. Applicant: Sopro. Device class: 2.

Clearance details

Applicant: Sopro
Product code: Code NBL
Device class: Class 2
Regulation: 21 CFR 872.1745
Advisory panel: Dental
Date received: 2009-08-21
Decision date: 2010-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mt. Laurel, NJ, US

Download summary PDF View on FDA.gov ↗

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K080122 — SOPRO 670 ARTHROSCOPIC PUMP2008-07-11

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