RESUBMITTED SCANORA— 510(k) K884650

Substantially Equivalent

Orion Corp.

FDA 510(k) clearance K884650 for RESUBMITTED SCANORA, Substantially Equivalent on 1989-03-16. Applicant: Orion Corp.. Device class: 2.

Clearance details

Applicant: Orion Corp.
Product code: Code IZF
Device class: Class 2
Regulation: 21 CFR 892.1740
Advisory panel: Radiology
Date received: 1988-11-07
Decision date: 1989-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: 20101 Turku, FI

Download summary PDF View on FDA.gov ↗

Recent devices under product code IZF

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K881506 — MAMEX DC MAG MG121988-06-10

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