STOPCOCK (ONE-PORT MANIFOLD)— 510(k) K934123

Substantially Equivalent

Merit Medical Systems, Inc.

FDA 510(k) clearance K934123 for STOPCOCK (ONE-PORT MANIFOLD), Substantially Equivalent on 1993-11-23. Applicant: Merit Medical Systems, Inc..

Clearance details

Applicant: Merit Medical Systems, Inc.
Product code: Code DTL
Advisory panel: Cardiovascular
Date received: 1993-08-25
Decision date: 1993-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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Adverse events under product code DTL

product code DTL

Malfunction: 770
Total: 770

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.