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 |