HVR PAIN RELIEF DEVICE— 510(k) K101716

Substantially Equivalent

H.V.R., Inc.

FDA 510(k) clearance K101716 for HVR PAIN RELIEF DEVICE, Substantially Equivalent on 2011-01-11. Applicant: H.V.R., Inc..

Clearance details

Applicant: H.V.R., Inc.
Product code: Code ILY
Advisory panel: Physical Medicine
Date received: 2010-06-18
Decision date: 2011-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Van Nuys, CA, US

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Adverse events under product code ILY

product code ILY

Death: 3
Total: 3

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.