MODIFICATION TO PROWESS PRO-SIM— 510(k) K984196
Substantially EquivalentSsgi Prowess Systems
FDA 510(k) clearance K984196 for MODIFICATION TO PROWESS PRO-SIM, Substantially Equivalent on 1998-12-11. Applicant: Ssgi Prowess Systems. Device class: 2.
Clearance details
- Applicant
- Ssgi Prowess Systems
- Product code
- Code MUJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.5050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Chico, CA, US
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