ANGIO DRAPE PACK ACP-010FM — Arrow Intl., Inc. (510(k) K880310)
ANGIO DRAPE PACK ACP-010FM — Arrow Intl., Inc. (510(k) K880310) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ANGIO DRAPE PACK ACP-010FM; Applicant: Arrow Intl., Inc.; Clearance track: 510(k).
| Device name | ANGIO DRAPE PACK ACP-010FM |
|---|---|
| Applicant | Arrow Intl., Inc. |
| Clearance track | 510(k) |
| Submission number | K880310 |
| Decision | Substantially Equivalent |
| Decision date | 1988-04-22 |
| Date received | 1988-01-25 |
| Product code | DXT |
| Device class | 2 |
| Medical specialty | Cardiovascular |
| Applicant location | PA, US |
| Source | openFDA device |
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$1999/mo
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