The following data is part of a premarket notification filed by Asahi Intecc Co., Ltd. with the FDA for Precious Plus Guide Catheter.
| Device ID | K072316 |
| 510k Number | K072316 |
| Device Name: | PRECIOUS PLUS GUIDE CATHETER |
| Classification | Catheter, Percutaneous |
| Applicant | ASAHI INTECC CO., LTD. 2500 RED HILL AVE, SUITE 210 Santa Ana, CA 92705 |
| Contact | Yoshi Terai |
| Correspondent | Yoshi Terai ASAHI INTECC CO., LTD. 2500 RED HILL AVE, SUITE 210 Santa Ana, CA 92705 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-08-17 |
| Decision Date | 2007-09-17 |
| Summary: | summary |