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 |