The following data is part of a premarket notification filed by Target Therapeutics with the FDA for Guider, Dasher.
| Device ID | K914030 |
| 510k Number | K914030 |
| Device Name: | GUIDER, DASHER |
| Classification | Wire, Guide, Catheter |
| Applicant | TARGET THERAPEUTICS 130 RIO ROBLES P.O. BOX 610458 San Jose, CA 95134 |
| Contact | Grace Brors |
| Correspondent | Grace Brors TARGET THERAPEUTICS 130 RIO ROBLES P.O. BOX 610458 San Jose, CA 95134 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-09-10 |
| Decision Date | 1992-02-11 |