STROBEX ULTRON ELECTROSURGE-DENTAL UNIT— 510(k) K850666

Name: FDA 510(k) clearance K850666
Creator: U.S. Food and Drug Administration
Published: 1985-05-29

Substantially Equivalent

Ipco Corp.

FDA 510(k) clearance K850666 for STROBEX ULTRON ELECTROSURGE-DENTAL UNIT, Substantially Equivalent on 1985-05-29. Applicant: Ipco Corp.. Device class: 2.

Clearance details

Applicant: Ipco Corp.
Product code: Code EKZ
Device class: Class 2
Regulation: 21 CFR 872.4920
Advisory panel: Dental
Date received: 1985-02-20
Decision date: 1985-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: White Plains, NY, US

Download summary PDF View on FDA.gov ↗

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