Artema Medical AB · Class I · Cleared Feb 21, 1995
| K-number | K945359 |
| Device name | AQUA+I-F, I-H, I-FH, II-H, II-FH, III-H |
| Applicant | Artema Medical AB |
| Product code | BYD |
| Device class | Class I |
| Decision date | Feb 21, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 868.5375 |
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