ACCESSORY TO UNIVERSAL OCTOPAQUE— 510(k) K930357

Name: FDA 510(k) clearance K930357
Creator: U.S. Food and Drug Administration
Published: 1993-07-13

Substantially Equivalent

Octostop, Inc.

FDA 510(k) clearance K930357 for ACCESSORY TO UNIVERSAL OCTOPAQUE, Substantially Equivalent on 1993-07-13. 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: 1993-01-26
Decision date: 1993-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Qc., CA

Download summary PDF View on FDA.gov ↗

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