FDA.report

Amanda Webb

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
96105203002808493Amanda Webb1N2020-04-253015 Carrington Mill Blvd. Morrisville NC US 27560
96126143002807495Amanda Webb1N2020-04-253015 Carrington Mill Blvd. Morrisville NC US 27560
30059462243005946224Amanda Webb1N2020-04-253015 Carrington Mill Blvd. Morrisville NC US 27560
30146445613014644561Amanda Webb1N2020-04-253015 Carrington Mill Blvd. Morrisville NC US 27560

Registered Device Listings

Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
228351630434850K993063RUSCH BRILLANT SILICONE FOLEYEZL1999-12-09
228351883395763K990619RUSCH REINFORCED ENDOTRACHEAL (OR TRACHEAL) TUBE- CUFFED AND UNCUFFED MURPHY/MAGILL, STERILEBTR1999-08-03
228351285330705K981203RUSCH BLAKEMORE 3 LUMEN, STERILEKNT1998-06-05
228351826985038K973892RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE)KNT1998-05-18
228351590040410K972184RUSCH BRILLANT SILICONE FOLEY CATHETEREZL1998-01-08
228351580360599K964056RUSCH ULTRA TRACHEOFLEX FENESTRATED KIT CUFFED,UNCUFFED/ RUSCH TRACHEOFLEX TRACHEOSTOMY KIT UNCUFFED STERILEJOH1997-10-10
228351100085941K955564RUSCH ULTRA TRACHEOFLEX TRACHEOSTOMY SET, CUFFED, STERILEJOH1996-06-28
228351898856062K955495RUSCH REINFORCED TRACHAEL TUBE CUFFED, STERILEBTR1996-06-27
228351450236890K935842RUSCH LASERTUBUS/RUSCH LASER RESISTANT CUFFED WITH MURPHY EYEBTR1995-05-23
1306701096899529K173596Rusch Intermittent Urethral CathetersEZC2018-01-29
228351096899529K173596Rusch Intermittent Urethral CathetersEZC2018-01-29
2208001007927144
228351022419292
1218531198116991
228351323392673
228351396497249
228351487961053
1306701487961053
228351564936978
228351784716747
228351793085890
228351842754061
228351865243022

Product Codes Associated With Registrations

Product codeRegistration listing recordsLatest decision
BTR31999-08-03
EZC22018-01-29
EZL21999-12-09
KNT21998-06-05
JOH21997-10-10