NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE— 510(k) K911970

Substantially Equivalent

Nasorcap Ent., Inc.

FDA 510(k) clearance K911970 for NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE, Substantially Equivalent on 1992-08-14. Applicant: Nasorcap Ent., Inc..

Clearance details

Applicant: Nasorcap Ent., Inc.
Product code: Code CCK
Advisory panel: Anesthesiology
Date received: 1991-05-03
Decision date: 1992-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Mifflin, PA, US

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Adverse events under product code CCK

product code CCK

Death: 3
Malfunction: 11,428
Total: 11,431

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.