Hospira, Inc. · Class II · Cleared Jun 26, 2006
| K-number | K061159 |
| Device name | OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH FLUIDIC SEAL WITH/WITHOUT HEPARIN |
| Applicant | Hospira, Inc. |
| Product code | DQE |
| Device class | Class II |
| Decision date | Jun 26, 2006 |
| Decision | Substantially Equivalent |
| Regulation | 870.1230 |
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