Quick Links: Skip to main page content
Skip to Search
Skip to Topics Menu
Skip to Common Links
U.S. Food & Drug Administration
Follow FDA
En Español
Search FDA
Home
Food
Drugs
Medical Devices
Radiation-Emitting Products
Vaccines, Blood & Biologics
Animal & Veterinary
Cosmetics
Tobacco Products
TPLC - Total Product Life Cycle
FDA Home
medical devices
databases
-
510(k)
|
DeNovo
|
Registration & Listing
|
Adverse Events
|
Recalls
|
PMA
|
HDE
|
Classification
|
Standards
CFR Title 21
|
Radiation-Emitting Products
|
X-Ray Assembler
|
Medsun Reports
|
CLIA
|
TPLC
New Search
show TPLC since
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
Back to Search Results
Device
lithotriptor, electro-hydraulic
Regulation Description
Electrohydraulic lithotriptor.
Product Code
FFK
Regulation Number
876.4480
Device Class
2
Premarket Reviews
Manufacturer
Decision
NORTHGATE TECHNOLOGIES INC.
SUBSTANTIALLY EQUIVALENT
1
WALZ ELEKTRONIK GMBH
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2020
39
39
2021
22
22
2022
13
13
2023
10
10
2024
8
8
2025
1
1
Device Problems
MDRs with this Device Problem
Events in those MDRs
Break
20
20
Output Problem
14
14
No Device Output
10
10
Detachment of Device or Device Component
10
10
Insufficient Information
8
8
Overheating of Device
6
6
Defective Device
5
5
Sparking
4
4
Electrical Power Problem
4
4
Adverse Event Without Identified Device or Use Problem
4
4
Activation Problem
3
3
Therapeutic or Diagnostic Output Failure
3
3
No Apparent Adverse Event
3
3
Tear, Rip or Hole in Device Packaging
3
3
Operating System Becomes Nonfunctional
2
2
Separation Problem
2
2
Mechanical Problem
2
2
Unintended Electrical Shock
2
2
Connection Problem
2
2
Failure to Power Up
2
2
Arcing of Electrodes
1
1
Improper or Incorrect Procedure or Method
1
1
Loose or Intermittent Connection
1
1
Electrical /Electronic Property Problem
1
1
Suction Problem
1
1
Appropriate Term/Code Not Available
1
1
Protective Measures Problem
1
1
Increase in Pressure
1
1
Device Contamination with Chemical or Other Material
1
1
Device Handling Problem
1
1
Material Deformation
1
1
Use of Device Problem
1
1
Misassembled During Installation
1
1
Defective Component
1
1
Smoking
1
1
Material Puncture/Hole
1
1
Material Erosion
1
1
Suction Failure
1
1
Image Display Error/Artifact
1
1
Communication or Transmission Problem
1
1
Fire
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
37
37
No Patient Involvement
21
21
No Consequences Or Impact To Patient
15
15
No Known Impact Or Consequence To Patient
4
4
Insufficient Information
4
4
Electric Shock
3
3
Perforation
2
2
Hepatitis
2
2
Bacterial Infection
2
2
Abdominal Pain
1
1
Hypovolemic Shock
1
1
Sepsis
1
1
No Information
1
1
Hematoma
1
1
Eye Burn
1
1
Fever
1
1
Foreign Body In Patient
1
1
Numbness
1
1
Hemorrhage/Bleeding
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Northgate Technologies, Inc.
II
Jun-03-2022
2
Northgate Technologies, Inc.
II
Dec-03-2021
3
Northgate Technologies, Inc.
II
Mar-24-2020
-
-