VARIANT OF OCTOSTOP AND OCTOPAQUE— 510(k) K930124

Name: FDA 510(k) clearance K930124
Creator: U.S. Food and Drug Administration
Published: 1994-02-09

Substantially Equivalent

Octostop, Inc.

FDA 510(k) clearance K930124 for VARIANT OF OCTOSTOP AND OCTOPAQUE, Substantially Equivalent on 1994-02-09. Applicant: Octostop, Inc.. Device class: 1.

Clearance details

Applicant: Octostop, Inc.
Product code: Code KXH
Device class: Class 1
Regulation: 21 CFR 892.1830
Advisory panel: Radiology
Date received: 1993-01-12
Decision date: 1994-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Qc., CA

Download summary PDF View on FDA.gov ↗

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