SORIN PULSE GENERATOR, MODEL #LIT-214— 510(k) K801640

Substantially Equivalent

Bentley Laboratories, Inc.

FDA 510(k) clearance K801640 for SORIN PULSE GENERATOR, MODEL #LIT-214, Substantially Equivalent on 1980-10-03. Applicant: Bentley Laboratories, Inc..

Clearance details

Applicant: Bentley Laboratories, Inc.
Product code: Code DXY
Advisory panel: Cardiovascular
Date received: 1980-07-17
Decision date: 1980-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DXY

product code DXY

Death: 240
Injury: 2,328
Malfunction: 2,096
Total: 4,664

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.