OXIMETER, IN VIVO CATHETER— 510(k) K760234
Substantially EquivalentOximetrix, Inc.
FDA 510(k) clearance K760234 for OXIMETER, IN VIVO CATHETER, Substantially Equivalent on 1976-08-23. Applicant: Oximetrix, Inc.. Device class: 2.
Clearance details
- Applicant
- Oximetrix, Inc.
- Product code
- Code DQE
- Device class
- Class 2
- Regulation
- 21 CFR 870.1230
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Oximetrix, Inc.
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