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.. Device class: 2.

Clearance details

Applicant: Orion Corp.
Product code: Code LQN
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1991-05-24
Decision date: 1992-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: 20101 Turku, FI

Download summary PDF View on FDA.gov ↗

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More clearances from Orion Corp.

K901637 — RESUBMITTED MODIFIED RUBALEX1990-04-26
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K890199 — DENTOCULT SM-STRIP MUTANS1989-03-02
K881505 — MAMEX DC MG111988-06-10
K881506 — MAMEX DC MAG MG121988-06-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.