UNIVERSAL INSTRU. SET FOR NEUROVASCULAR— 510(k) K831071

Substantially Equivalent

Prothia USA, Inc.

FDA 510(k) clearance K831071 for UNIVERSAL INSTRU. SET FOR NEUROVASCULAR, Substantially Equivalent on 1983-06-08. Applicant: Prothia USA, Inc..

Clearance details

Applicant: Prothia USA, Inc.
Product code: Code GZX
Advisory panel: Neurology
Date received: 1983-04-04
Decision date: 1983-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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