RUBALEX, MODIFICATION— 510(k) K912391

Substantially Equivalent

Orion Corp.

FDA 510(k) clearance K912391 for RUBALEX, MODIFICATION, Substantially Equivalent on 1992-05-04. Applicant: Orion Corp..

Clearance details

Applicant: Orion Corp.
Product code: Code LQN
Advisory panel: Microbiology
Date received: 1991-05-24
Decision date: 1992-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: 20101 Turku, FI

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