LEE ASPIRATION NEEDLE— 510(k) K771574
Substantially EquivalentRadiation Development Co., Inc.
FDA 510(k) clearance K771574 for LEE ASPIRATION NEEDLE, Substantially Equivalent on 1977-12-06. Applicant: Radiation Development Co., Inc..
Clearance details
- Applicant
- Radiation Development Co., Inc.
- Product code
- Code GDM
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Adverse events under product code GDM
product code GDM- Death
- 2
- Total
- 2
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.