TUBING, POLYETHYLENE — Coeur Laboratories, Inc. (510(k) K873597)
TUBING, POLYETHYLENE — Coeur Laboratories, Inc. (510(k) K873597) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: TUBING, POLYETHYLENE; Applicant: Coeur Laboratories, Inc.; Clearance track: 510(k).
| Device name | TUBING, POLYETHYLENE |
|---|---|
| Applicant | Coeur Laboratories, Inc. |
| Clearance track | 510(k) |
| Submission number | K873597 |
| Decision | Substantially Equivalent |
| Decision date | 1987-11-12 |
| Date received | 1987-09-04 |
| Product code | DXT |
| Device class | 2 |
| Medical specialty | Cardiovascular |
| Applicant location | NC, US |
| Source | openFDA device |
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