ULTRABLOX— 510(k) K133684

Substantially Equivalent

Bloxr Corporation

FDA 510(k) clearance K133684 for ULTRABLOX, Substantially Equivalent on 2014-01-13. Applicant: Bloxr Corporation. Device class: 2.

Clearance details

Applicant: Bloxr Corporation
Product code: Code PDK
Device class: Class 2
Regulation: 21 CFR 892.6510
Advisory panel: Radiology
Date received: 2013-12-02
Decision date: 2014-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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