AUDICOR SENSOR-ADAPTER MODEL AUDICOR SENSOR-ADAPTER 4.0— 510(k) K103516
Substantially EquivalentInovise Medical, Inc.
FDA 510(k) clearance K103516 for AUDICOR SENSOR-ADAPTER MODEL AUDICOR SENSOR-ADAPTER 4.0, Substantially Equivalent on 2011-02-04. Applicant: Inovise Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Inovise Medical, Inc.
- Product code
- Code DQD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Beaverton, OR, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.