Spectramed, Inc. · Class II · Cleared Jan 19, 1990
| K-number | K896122 |
| Device name | AMNICATHDL(TM) DT-IUPC2 DUAL LUMEN TRANS. TIPPED |
| Applicant | Spectramed, Inc. |
| Product code | KXO |
| Device class | Class II |
| Decision date | Jan 19, 1990 |
| Decision | Substantially Equivalent |
| Regulation | 884.2700 |
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