The following data is part of a premarket notification filed by Quest Medical, Inc. with the FDA for Catheter Guide Wire.
| Device ID | K820699 |
| 510k Number | K820699 |
| Device Name: | CATHETER GUIDE WIRE |
| Classification | Wire, Guide, Catheter |
| Applicant | QUEST MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-03-15 |
| Decision Date | 1982-04-09 |