VITEL III, ECG TRANSMITTER— 510(k) K872229

Substantially Equivalent

Equimed Corp.

FDA 510(k) clearance K872229 for VITEL III, ECG TRANSMITTER, Substantially Equivalent on 1987-07-29. Applicant: Equimed Corp..

Clearance details

Applicant: Equimed Corp.
Product code: Code DSH
Advisory panel: Cardiovascular
Date received: 1987-06-09
Decision date: 1987-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plymouth, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DSH

product code DSH

Death: 3
Injury: 652
Total: 655

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.