SANPO I— 510(k) K964541
Substantially EquivalentKoike Medical Co.
FDA 510(k) clearance K964541 for SANPO I, Substantially Equivalent on 1997-09-26. Applicant: Koike Medical Co.. Device class: 2.
Clearance details
- Applicant
- Koike Medical Co.
- Product code
- Code NFB
- Device class
- Class 2
- Regulation
- 21 CFR 868.5905
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code NFB
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