The following data is part of a premarket notification filed by Cathera, Inc. with the FDA for Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter.
Device ID | K151638 |
510k Number | K151638 |
Device Name: | Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter |
Classification | Catheter, Percutaneous |
Applicant | Cathera, Inc. 627 National Ave. Mountain View, CA 94043 |
Contact | Victor Ham |
Correspondent | Victor Ham Cathera, Inc. 627 National Ave. Mountain View, CA 94043 |
Product Code | DQY |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-06-17 |
Decision Date | 2015-11-13 |
Summary: | summary |