SIEMENS SIRESKOP 4— 510(k) K820111
Substantially EquivalentSiemens Corp.
FDA 510(k) clearance K820111 for SIEMENS SIRESKOP 4, Substantially Equivalent on 1982-02-18. Applicant: Siemens Corp.. Device class: 2.
Clearance details
- Applicant
- Siemens Corp.
- Product code
- Code KXJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.1980
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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