SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6— 510(k) K071204

Substantially Equivalent

C.R. Bard, Inc.

FDA 510(k) clearance K071204 for SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6, Substantially Equivalent on 2007-05-18. Applicant: C.R. Bard, Inc..

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code IYO
Advisory panel: Radiology
Date received: 2007-05-01
Decision date: 2007-05-18
Decision: Substantially Equivalent
Clearance type: Special
Location: Salt Lake City, UT, US

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Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.