BALT GUIDING CATHETER — Target Therapeutics (510(k) K925632)
BALT GUIDING CATHETER — Target Therapeutics (510(k) K925632) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: BALT GUIDING CATHETER; Applicant: Target Therapeutics; Clearance track: 510(k).
| Device name | BALT GUIDING CATHETER |
|---|---|
| Applicant | Target Therapeutics |
| Clearance track | 510(k) |
| Submission number | K925632 |
| Decision | Substantially Equivalent |
| Decision date | 1993-06-29 |
| Date received | 1992-11-09 |
| Product code | DQO |
| Device class | 2 |
| Medical specialty | Cardiovascular |
| Applicant location | CA, US |
| Source | openFDA device |
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