ANGIOPLASTY BALLOON INFLATION DEVICE— 510(k) K880158

Substantially Equivalent

L.O.N. Research, Inc.

FDA 510(k) clearance K880158 for ANGIOPLASTY BALLOON INFLATION DEVICE, Substantially Equivalent on 1988-03-22. Applicant: L.O.N. Research, Inc..

Clearance details

Applicant: L.O.N. Research, Inc.
Product code: Code LIT
Advisory panel: Cardiovascular
Date received: 1988-01-13
Decision date: 1988-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sanford, FL, US

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Adverse events under product code LIT

product code LIT

Death: 27
Injury: 1,256
Malfunction: 12,127
Total: 13,410

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.