MERIDIAN MEDICAL SYSTEMS VOLUME VENTILATOR CIRCUIT— 510(k) K925262

Substantially Equivalent

Merit Medical Systems, Inc.

FDA 510(k) clearance K925262 for MERIDIAN MEDICAL SYSTEMS VOLUME VENTILATOR CIRCUIT, Substantially Equivalent on 1993-01-22. Applicant: Merit Medical Systems, Inc..

Clearance details

Applicant: Merit Medical Systems, Inc.
Product code: Code CBK
Advisory panel: Anesthesiology
Date received: 1992-10-19
Decision date: 1993-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

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Adverse events under product code CBK

product code CBK

Death: 736
Injury: 3,628
Malfunction: 98,786
Other: 4
Total: 103,154

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.