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 |