DENVER PERITONEO-VENOUS SHUNT (DP-VS)— 510(k) K822686
Substantially EquivalentDenver Biomedicals, Inc.
FDA 510(k) clearance K822686 for DENVER PERITONEO-VENOUS SHUNT (DP-VS), Substantially Equivalent on 1982-09-21. Applicant: Denver Biomedicals, Inc.. Device class: 2.
Clearance details
- Applicant
- Denver Biomedicals, Inc.
- Product code
- Code KPM
- Device class
- Class 2
- Regulation
- 21 CFR 876.5955
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.