The following data is part of a premarket notification filed by Shiley, Inc. with the FDA for Schneider-shiley Guide Wire.
| Device ID | K864787 |
| 510k Number | K864787 |
| Device Name: | SCHNEIDER-SHILEY GUIDE WIRE |
| Classification | Wire, Guide, Catheter |
| Applicant | SHILEY, INC. 17600 GILLETTE AVE. P.O. BOX 19503 Irvine, CA 92714 |
| Contact | Morton Barak |
| Correspondent | Morton Barak SHILEY, INC. 17600 GILLETTE AVE. P.O. BOX 19503 Irvine, CA 92714 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-12-08 |
| Decision Date | 1987-02-19 |