LIBERATOR 53/STROLLER 50— 510(k) K880101

Substantially Equivalent

Minnesota Valley Engineering, Inc.

FDA 510(k) clearance K880101 for LIBERATOR 53/STROLLER 50, Substantially Equivalent on 1988-02-29. Applicant: Minnesota Valley Engineering, Inc..

Clearance details

Applicant: Minnesota Valley Engineering, Inc.
Product code: Code BYJ
Advisory panel: Anesthesiology
Date received: 1988-01-12
Decision date: 1988-02-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Prague, MN, US

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Adverse events under product code BYJ

product code BYJ

Death: 16
Total: 16

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.