DENVER PLEURO-PERITONEAL SHUNT— 510(k) K880570
Substantially EquivalentCodman & Shurtleff, Inc.
FDA 510(k) clearance K880570 for DENVER PLEURO-PERITONEAL SHUNT, Substantially Equivalent on 1988-06-20. Applicant: Codman & Shurtleff, Inc.. Device class: 2.
Clearance details
- Applicant
- Codman & Shurtleff, 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
- Randolph, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.