MONITOR, PO2, INTRAVASCULAR— 510(k) K781271
Substantially EquivalentRoche Medical Electronics, Inc.
FDA 510(k) clearance K781271 for MONITOR, PO2, INTRAVASCULAR, Substantially Equivalent on 1978-10-12. Applicant: Roche Medical Electronics, Inc.. Device class: 2.
Clearance details
- Applicant
- Roche Medical Electronics, Inc.
- Product code
- Code CCE
- Device class
- Class 2
- Regulation
- 21 CFR 868.1200
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Recent devices under product code CCE
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