The following data is part of a premarket notification filed by Baylis Medical Company Inc. with the FDA for Protrack Rf Anchor Wire.
| Device ID | K150709 |
| 510k Number | K150709 |
| Device Name: | ProTrack RF Anchor Wire |
| Classification | Catheter, Septostomy |
| Applicant | BAYLIS MEDICAL COMPANY INC. 2645 MATHESON BLVD. EAST Mississauga, CA L4w 5s4 |
| Contact | Meghal Khakhar |
| Correspondent | Meghal Khakhar BAYLIS MEDICAL COMPANY INC. 2645 MATHESON BLVD. EAST Mississauga, CA L4w 5s4 |
| Product Code | DXF |
| CFR Regulation Number | 870.5175 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-03-19 |
| Decision Date | 2015-06-17 |
| Summary: | summary |