The following data is part of a premarket notification filed by Teleflex, Inc. with the FDA for Flextip Plus Closed Tip Epidural Catherter.
Device ID | K103658 |
510k Number | K103658 |
Device Name: | FLEXTIP PLUS CLOSED TIP EPIDURAL CATHERTER |
Classification | Anesthesia Conduction Kit |
Applicant | TELEFLEX, INC. 2400 BERNVILLE ROAD Reading, PA 19605 |
Contact | Paul Amudala |
Correspondent | Paul Amudala TELEFLEX, INC. 2400 BERNVILLE ROAD Reading, PA 19605 |
Product Code | CAZ |
CFR Regulation Number | 868.5140 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-12-15 |
Decision Date | 2012-05-16 |
Summary: | summary |