The following data is part of a premarket notification filed by Mallinckrodt Medical with the FDA for Percutaneous Transluminal Angioplasty Guidewire.
| Device ID | K905548 |
| 510k Number | K905548 |
| Device Name: | PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY GUIDEWIRE |
| Classification | Wire, Guide, Catheter |
| Applicant | MALLINCKRODT MEDICAL 675 MCDONNELL BLVD. P.O. BOX 5840 St. Louis, MO 63134 |
| Contact | David E Brown |
| Correspondent | David E Brown MALLINCKRODT MEDICAL 675 MCDONNELL BLVD. P.O. BOX 5840 St. Louis, MO 63134 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-12-11 |
| Decision Date | 1991-02-25 |