The following data is part of a premarket notification filed by Ivy Biomedical Systems, Inc. with the FDA for Cardiac Trigger Monitor.
Device ID | K110987 |
510k Number | K110987 |
Device Name: | CARDIAC TRIGGER MONITOR |
Classification | Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm) |
Applicant | IVY BIOMEDICAL SYSTEMS, INC. 11 BUSINESS PARK DR. Branford, CT 06405 |
Contact | Dick Listro |
Correspondent | Dick Listro IVY BIOMEDICAL SYSTEMS, INC. 11 BUSINESS PARK DR. Branford, CT 06405 |
Product Code | DRT |
CFR Regulation Number | 870.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-04-08 |
Decision Date | 2011-07-22 |