POINTER F-3— 510(k) K833037

Substantially Equivalent

Petra Intl. Co.

FDA 510(k) clearance K833037 for POINTER F-3, Substantially Equivalent on 1983-11-29. Applicant: Petra Intl. Co.. Device class: 2.

Clearance details

Applicant: Petra Intl. Co.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1983-09-07
Decision date: 1983-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.