FDA 510(k) Applications Submitted by LORI PFOHL
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K180253 |
01/30/2018 |
Sheridan Endobronchial Tubes |
Teleflex Medical |
| K130405 |
02/19/2013 |
RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET |
TELEFLEX MEDICAL |
| K150603 |
03/10/2015 |
Rusch Safety Silk Pediatric Series Oral/Nasal Tracheal Tube |
Teleflex Medical, Inc. |
| K161770 |
06/28/2016 |
Rusch Silicone Foley Catheter |
Teleflex Medical, Inc. |
| K141888 |
07/14/2014 |
RUSCH ENDOBRONCHIAL TUBES |
Teleflex Medical, Inc. |
| K122235 |
07/26/2012 |
RUSCH TRACFLEX PLUS TRACHEOSTOMY TUBE SET |
Teleflex Medical, Inc. |
| K132415 |
08/02/2013 |
RUSCH SAFETY SILK SERIES ORAL/NASAL TRACHEAL TUBE |
Teleflex Medical, Inc. |
| K192324 |
08/27/2019 |
Sheridan Spiral-Flex Endotracheal Tubes |
TeleflexMedical, Inc |
| K133173 |
10/17/2013 |
RUSCH TRACFLEX PLUS PEDIATRIC TRACHEOSTOMY TUBE SET |
Teleflex Medical, Inc. |
| K162989 |
10/27/2016 |
Rusch Simplastic Foley Catheters |
TELEFLEX MEDICAL, INC. |
| K183461 |
12/14/2018 |
Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter |
Teleflex Medical, Inc |
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