The following data is part of a premarket notification filed by Merit Medical Systems, Inc. with the FDA for Concierge Guiding Catheter.
Device ID | K132409 |
510k Number | K132409 |
Device Name: | CONCIERGE GUIDING CATHETER |
Classification | Catheter, Percutaneous |
Applicant | MERIT MEDICAL SYSTEMS, INC. 1600 WEST MERIT PKWY. South Jordan, UT 84095 |
Contact | Vicki Godwin |
Correspondent | Vicki Godwin MERIT MEDICAL SYSTEMS, INC. 1600 WEST MERIT PKWY. South Jordan, UT 84095 |
Product Code | DQY |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-08-02 |
Decision Date | 2013-08-29 |
Summary: | summary |