CURIETRON 192 LOW DOSE RATE— 510(k) K881323

Name: FDA 510(k) clearance K881323
Creator: U.S. Food and Drug Administration
Published: 1989-01-17

Substantially Equivalent

Compagnie Oris Industrie, S.A.

FDA 510(k) clearance K881323 for CURIETRON 192 LOW DOSE RATE, Substantially Equivalent on 1989-01-17. Applicant: Compagnie Oris Industrie, S.A.. Device class: 2.

Clearance details

Applicant: Compagnie Oris Industrie, S.A.
Product code: Code JAQ
Device class: Class 2
Regulation: 21 CFR 892.5700
Advisory panel: Radiology
Date received: 1988-03-28
Decision date: 1989-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: France, FR

Download summary PDF View on FDA.gov ↗

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