The following data is part of a premarket notification filed by Meadox Surgimed, Inc. with the FDA for Quickwire - Hydrophilic Coated Guidewire.
| Device ID | K904582 |
| 510k Number | K904582 |
| Device Name: | QUICKWIRE - HYDROPHILIC COATED GUIDEWIRE |
| Classification | Wire, Guide, Catheter |
| Applicant | MEADOX SURGIMED, INC. 112 BAUER DR. Oakland, NJ 07436 |
| Contact | Patricia G Scharf |
| Correspondent | Patricia G Scharf MEADOX SURGIMED, INC. 112 BAUER DR. Oakland, NJ 07436 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-09 |
| Decision Date | 1991-02-25 |