Concord/Portex · Class I · Cleared Jun 22, 1993
| K-number | K930286 |
| Device name | DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS |
| Applicant | Concord/Portex |
| Product code | CBT |
| Device class | Class I |
| Decision date | Jun 22, 1993 |
| Decision | Substantially Equivalent — Kit Device |
| Regulation | 868.1100 |
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