Matrix Medica, Inc. · Class II · Cleared Feb 17, 1989
| K-number | K883833 |
| Device name | NITRONOX(R), FIRST RESPONSE NITRONOX(TM) |
| Applicant | Matrix Medica, Inc. |
| Product code | BZR |
| Device class | Class II |
| Decision date | Feb 17, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 868.5330 |
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