GE TARGET SERIES 2— 510(k) K896353

Substantially Equivalent

GE Medical Systems

FDA 510(k) clearance K896353 for GE TARGET SERIES 2, Substantially Equivalent on 1989-12-22. Applicant: GE Medical Systems. Device class: 2.

Clearance details

Applicant: GE Medical Systems
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1989-11-06
Decision date: 1989-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, 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.