SIREDOC 60 AND SIREDOC 220— 510(k) K863331
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K863331 for SIREDOC 60 AND SIREDOC 220, Substantially Equivalent on 1986-10-06. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 1.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code DSF
- Device class
- Class 1
- Regulation
- 21 CFR 870.2810
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Iselin, NJ, US
Recent devices under product code DSF
view allMore clearances from Siemens Medical Solutions USA, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.