The following data is part of a premarket notification filed by Target Therapeutics with the FDA for Taper Guidewires.
| Device ID | K924987 |
| 510k Number | K924987 |
| Device Name: | TAPER GUIDEWIRES |
| Classification | Wire, Guide, Catheter |
| Applicant | TARGET THERAPEUTICS 47201 LAKEVIEW BLVD. P.O. BOX 5120 Freemont, CA 94538 |
| Contact | Craig J Coombs |
| Correspondent | Craig J Coombs TARGET THERAPEUTICS 47201 LAKEVIEW BLVD. P.O. BOX 5120 Freemont, CA 94538 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-10-14 |
| Decision Date | 1992-12-08 |