LIFESCOPE II — Nihon Kohden America, Inc. (510(k) K841499)
LIFESCOPE II — Nihon Kohden America, Inc. (510(k) K841499) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: LIFESCOPE II; Applicant: Nihon Kohden America, Inc.; Clearance track: 510(k).
| Device name | LIFESCOPE II |
|---|---|
| Applicant | Nihon Kohden America, Inc. |
| Clearance track | 510(k) |
| Submission number | K841499 |
| Decision | Substantially Equivalent |
| Decision date | 1984-08-28 |
| Date received | 1984-04-10 |
| Product code | DRT |
| Device class | 2 |
| Medical specialty | Cardiovascular |
| Applicant location | CA, US |
| Source | openFDA device |
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