The following data is part of a premarket notification filed by Clinical Innovations, Llc with the FDA for Ebb Complete Tamponade System.
Device ID | K150573 |
510k Number | K150573 |
Device Name: | Ebb Complete Tamponade System |
Classification | Intrauterine Tamponade Balloon |
Applicant | CLINICAL INNOVATIONS, LLC 747 WEST 4170 SOUTH Murray, UT 84123 |
Contact | Tom Haueter |
Correspondent | Tom Haueter CLINICAL INNOVATIONS, LLC 747 WEST 4170 SOUTH Murray, UT 84123 |
Product Code | OQY |
CFR Regulation Number | 884.4530 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-03-06 |
Decision Date | 2015-03-25 |
Summary: | summary |