VERAPLUG— 510(k) K140352

Name: FDA 510(k) clearance K140352
Creator: U.S. Food and Drug Administration
Published: 2014-11-13

Substantially Equivalent

Krishna Imports Inc Dba Stephens Instruments

FDA 510(k) clearance K140352 for VERAPLUG, Substantially Equivalent on 2014-11-13. Applicant: Krishna Imports Inc Dba Stephens Instruments. Device class: Unclassified.

Clearance details

Applicant: Krishna Imports Inc Dba Stephens Instruments
Product code: Code LZU
Device class: Unclassified
Advisory panel: Unknown
Date received: 2014-02-12
Decision date: 2014-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lexington, KY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LZU

product code LZU

Other: 2
Total: 2

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.