ProdiGI— 510(k) DEN220006
UnknownCovidien, LLC
FDA 510(k) clearance DEN220006 for ProdiGI, Unknown on 2022-06-13. Applicant: Covidien, LLC. Device class: 2.
Clearance details
- Applicant
- Covidien, LLC
- Product code
- Code QSW
- Device class
- Class 2
- Regulation
- 21 CFR 876.4410
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Santa Clara, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.