FLOTEC OXYSAVRR (S)— 510(k) K970371
Substantially EquivalentFlotec, Inc.
FDA 510(k) clearance K970371 for FLOTEC OXYSAVRR (S), Substantially Equivalent on 1997-07-10. Applicant: Flotec, Inc.. Device class: 2.
Clearance details
- Applicant
- Flotec, Inc.
- 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
- Indianapolis, IN, US
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