CANNULA, INTRAVENOUS, R— 510(k) K770512

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K770512 for CANNULA, INTRAVENOUS, R, Substantially Equivalent on 1977-03-30. Applicant: Sherwood Medical Industries.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code DQR
Advisory panel: Cardiovascular
Date received: 1977-03-17
Decision date: 1977-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DQR

product code DQR

Death: 2
Total: 2

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.