The following data is part of a premarket notification filed by Shiley, Inc. with the FDA for Shiley Silicone Sual Lumen Subclavian Cannual.
| Device ID | K852070 |
| 510k Number | K852070 |
| Device Name: | SHILEY SILICONE SUAL LUMEN SUBCLAVIAN CANNUAL |
| Classification | Catheter, Subclavian |
| Applicant | SHILEY, INC. 17600 GILLETTE AVE. P.O. BOX 19503 Irvine, CA 92714 |
| Contact | Ron Duchene |
| Correspondent | Ron Duchene SHILEY, INC. 17600 GILLETTE AVE. P.O. BOX 19503 Irvine, CA 92714 |
| Product Code | LFJ |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-05-10 |
| Decision Date | 1985-06-13 |