EXTERNAL PULSE GENERATOR FOR TEMP. STIM— 510(k) K831768

Substantially Equivalent

Oscor, Inc.

FDA 510(k) clearance K831768 for EXTERNAL PULSE GENERATOR FOR TEMP. STIM, Substantially Equivalent on 1983-12-16. Applicant: Oscor, Inc..

Clearance details

Applicant: Oscor, Inc.
Product code: Code DTE
Advisory panel: Cardiovascular
Date received: 1983-06-01
Decision date: 1983-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palm Harbor, FL, US

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Adverse events under product code DTE

product code DTE

Death: 18
Injury: 247
Malfunction: 4,603
Total: 4,868

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.