AMBU TUBECHECK — Ambu, Inc. (510(k) K981891)
AMBU TUBECHECK — Ambu, Inc. (510(k) K981891) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: AMBU TUBECHECK; Applicant: Ambu, Inc.; Clearance track: 510(k).
| Device name | AMBU TUBECHECK |
|---|---|
| Applicant | Ambu, Inc. |
| Clearance track | 510(k) |
| Submission number | K981891 |
| Decision | Substantially Equivalent |
| Decision date | 1998-07-17 |
| Date received | 1998-05-29 |
| Product code | BTR |
| Device class | 2 |
| Medical specialty | Anesthesiology |
| Applicant location | MD, US |
| Source | openFDA device |
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