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 |