MINISCOPE MS-3— 510(k) K954066

Substantially Equivalent

Schiller America, Inc.

FDA 510(k) clearance K954066 for MINISCOPE MS-3, Substantially Equivalent on 1995-10-27. Applicant: Schiller America, Inc..

Clearance details

Applicant: Schiller America, Inc.
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 1995-08-30
Decision date: 1995-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

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Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

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.