ROBERTSITE STOPCOCK— 510(k) K061143

Name: FDA 510(k) clearance K061143
Creator: U.S. Food and Drug Administration
Published: 2006-05-10

Substantially Equivalent

Halkey-Roberts Corp.

FDA 510(k) clearance K061143 for ROBERTSITE STOPCOCK, Substantially Equivalent on 2006-05-10. Applicant: Halkey-Roberts Corp.. Device class: 2.

Clearance details

Applicant: Halkey-Roberts Corp.
Product code: Code FMG
Device class: Class 2
Regulation: 21 CFR 880.5440
Advisory panel: General Hospital
Date received: 2006-04-25
Decision date: 2006-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Petersburg, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FMG

product code FMG

Death: 14
Malfunction: 3,433
Other: 1
Total: 3,448

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.