VIEWING CLIENT MOBILE— 510(k) K141536

Substantially Equivalent

Axon Medical Technologies Corp.

FDA 510(k) clearance K141536 for VIEWING CLIENT MOBILE, Substantially Equivalent on 2015-03-06. Applicant: Axon Medical Technologies Corp..

Clearance details

Applicant: Axon Medical Technologies Corp.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2014-06-10
Decision date: 2015-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toronto, Ontario, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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