MORSE DT MANIFOLD— 510(k) K902472

Substantially Equivalent

North American Instrument Corp.

FDA 510(k) clearance K902472 for MORSE DT MANIFOLD, Substantially Equivalent on 1990-08-23. Applicant: North American Instrument Corp..

Clearance details

Applicant: North American Instrument Corp.
Product code: Code DRS
Advisory panel: Cardiovascular
Date received: 1990-06-04
Decision date: 1990-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glens Falls, NY, 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.