ULTRALITH ULTRASONIC LITHOTRIPSY SYSTEM— 510(k) K850298
Substantially EquivalentCabot Medical Corp.
FDA 510(k) clearance K850298 for ULTRALITH ULTRASONIC LITHOTRIPSY SYSTEM, Substantially Equivalent on 1985-03-05. Applicant: Cabot Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Cabot Medical Corp.
- Product code
- Code FEO
- Device class
- Class 2
- Regulation
- 21 CFR 876.4480
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Langhorne, PA, US
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Adverse events under product code FEO
product code FEO- Malfunction
- 910
- Other
- 1
- Total
- 911
Source: openFDA MAUDE database, through . 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.