DISPOS. MONITORING SYS/LI ET AL— 510(k) K820201

Substantially Equivalent

Linton Biomed Corp.

FDA 510(k) clearance K820201 for DISPOS. MONITORING SYS/LI ET AL, Substantially Equivalent on 1982-02-12. Applicant: Linton Biomed Corp..

Clearance details

Applicant: Linton Biomed Corp.
Product code: Code DRS
Advisory panel: Cardiovascular
Date received: 1982-01-26
Decision date: 1982-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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Adverse events under product code DRS

product code DRS

Death: 8
Malfunction: 776
Total: 784

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.