QUIKPAGE ARRHYTHMIA REPORT GENERATOR — Agilent Technologies (510(k) K841083)
QUIKPAGE ARRHYTHMIA REPORT GENERATOR — Agilent Technologies (510(k) K841083) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: QUIKPAGE ARRHYTHMIA REPORT GENERATOR; Applicant: Agilent Technologies; Clearance track: 510(k).
| Device name | QUIKPAGE ARRHYTHMIA REPORT GENERATOR |
|---|---|
| Applicant | Agilent Technologies |
| Clearance track | 510(k) |
| Submission number | K841083 |
| Decision | Substantially Equivalent |
| Decision date | 1985-02-07 |
| Date received | 1984-03-13 |
| Product code | DSI |
| Device class | 2 |
| Medical specialty | Cardiovascular |
| Applicant location | CA, US |
| Source | openFDA device |
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$1999/mo
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