DYNACAD/PROSTATE INTERVENTIONAL (DYNALOC/PROSTATE)— 510(k) K133030

Substantially Equivalent

Invivo Corporation

FDA 510(k) clearance K133030 for DYNACAD/PROSTATE INTERVENTIONAL (DYNALOC/PROSTATE), Substantially Equivalent on 2014-01-22. Applicant: Invivo Corporation.

Clearance details

Applicant: Invivo Corporation
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2013-09-26
Decision date: 2014-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Florida, FL, US

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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.