The following data is part of a premarket notification filed by Creagh Medical, Ltd. with the FDA for 018 Hydrophilic Coated Otw Pta Balloon Dilatation Catheter.
Device ID | K180007 |
510k Number | K180007 |
Device Name: | 018 Hydrophilic Coated OTW PTA Balloon Dilatation Catheter |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | Creagh Medical, Ltd. IDA Business Park Ballinasloe, IE H53 K8p4 |
Contact | Shane Costello |
Correspondent | Sherri Mellingen dba Surmodics, Inc. 9924 West 74th Street Eden Prairie, MN 55344 |
Product Code | LIT |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-01-02 |
Decision Date | 2018-04-19 |
Summary: | summary |