REGULUS NAVIGATOR — Compass Intl., Inc. (510(k) K964229)
REGULUS NAVIGATOR — Compass Intl., Inc. (510(k) K964229) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: REGULUS NAVIGATOR; Applicant: Compass Intl., Inc.; Clearance track: 510(k).
| Device name | REGULUS NAVIGATOR |
|---|---|
| Applicant | Compass Intl., Inc. |
| Clearance track | 510(k) |
| Submission number | K964229 |
| Decision | Substantially Equivalent |
| Decision date | 1997-08-19 |
| Date received | 1996-10-23 |
| Product code | HAW |
| Device class | 2 |
| Medical specialty | Neurology |
| Applicant location | MN, US |
| Source | openFDA device |
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$1999/mo
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