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FDA 510(k) Applications Submitted by DAVID H MUELLER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K971756
05/12/1997
MEDTRONIC MODEL 3998 LEAD
MEDTRONIC VASCULAR
K011584
05/23/2001
MEDTRONIC SPINAL CORD STIMULATION AND PERIPHERAL NERVE STIMULATION SYSTEMS FOR PAIN RELIEF
MEDTRONIC VASCULAR
K972043
06/02/1997
MEDTRONIC MODEL 3273/3274 RF RECEIVER AND MODEL 3629/3630 SCREENER
MEDTRONIC VASCULAR
K972906
08/06/1997
MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA)
MEDTRONIC VASCULAR
K953742
08/08/1995
BIFURCATED Y-EXTENSION
MEDTRONIC VASCULAR
K982902
08/14/1998
PERIPHERAL NERVE STIMULATION
MEDTRONIC VASCULAR
K222983
09/28/2022
NeuroBlate Fusion-S Software V3.17
Monteris Medical,
K964172
10/18/1996
MEDTRONIC MODEL 3991A, 3992A, 3993A, 3994A LEADS OR TRANSVERSE TRIPOLAR LEADS OR TTL
MEDTRONIC VASCULAR
K170724
03/09/2017
NeuroBlate System
Monteris Medical
K201056
04/21/2020
NeuroBlate System
Monteris Medical, Inc.
K171255
04/28/2017
Monteris Medical NeuroBlate System
Monteris Medical, Inc.
K182036
07/30/2018
NeuroBlate System
Monteris Medical
K172881
09/21/2017
NeuroBlate System
Monteris Medical
K162762
09/30/2016
NeuroBlate System
Monteris Medical, Inc.
K173305
10/18/2017
NeuroBlate System
Monteris Medical,
K193375
12/05/2019
NeuroBlate System
Monteris Medical
K041884
07/12/2004
MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS
MUELLER WATER CONDITIONING, INC.
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