The following data is part of a premarket notification filed by Teleflex, Inc. with the FDA for Flextip Plus Epidural Catheter;flexblock Continous Peripheral Nerve Block Catheter Kit/set.
| Device ID | K140110 |
| 510k Number | K140110 |
| Device Name: | FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET |
| Classification | Catheter, Conduction, Anesthetic |
| Applicant | TELEFLEX, INC. 2400 BERNVILLE ROAD Reading, PA 19605 |
| Contact | Chet Jones |
| Correspondent | Chet Jones TELEFLEX, INC. 2400 BERNVILLE ROAD Reading, PA 19605 |
| Product Code | BSO |
| CFR Regulation Number | 868.5120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-01-15 |
| Decision Date | 2015-03-27 |
| Summary: | summary |