The following data is part of a premarket notification filed by Advanced Cardiovascular Systems, Inc. with the FDA for Acs 0.025-in Hi-torq Modif J/stand Telesc Guidewir.
| Device ID | K874776 |
| 510k Number | K874776 |
| Device Name: | ACS 0.025-IN HI-TORQ MODIF J/STAND TELESC GUIDEWIR |
| Classification | Wire, Guide, Catheter |
| Applicant | ADVANCED CARDIOVASCULAR SYSTEMS, INC. 1395 CHARLESTON RD. Mountain View, CA 94043 |
| Contact | Marianna Faist |
| Correspondent | Marianna Faist ADVANCED CARDIOVASCULAR SYSTEMS, INC. 1395 CHARLESTON RD. Mountain View, CA 94043 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-19 |
| Decision Date | 1988-02-17 |