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Extracorporeal Acoustic Wave Generating Accessory To Urological Indwelling Catheter For Use During Public Health Emergen

Page Type
Product Code
Definition
The device is an acoustic wave generating extracorporeal accessory to indwelling urinary catheters intended to aid in the reduction of catheter-associated urinary tract infection (CAUTI) incidence in patients requiring long-term (= 14 days) indwelling catheterization. Intended for use during declared public health emergency.
Physical State
Battery powered driver unit and vibration actuator connected to an indwelling urological catheter.
Technical Method
To deliver acoustic waves to reduce bacterial attachment on the inner and outer surfaces of the indwelling urinary catheter.
Target Area
Intraurethral mucosal tissue surrounding, and inner and outer surfaces of an indwelling catheter.
Review Panel
Gastroenterology and Urology
Submission Type
Enforcement Discretion
Device Classification
N
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

As product code QMK is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.

Extracorporeal Acoustic Wave Generating Accessory To Urological Indwelling Catheter For Use During Public Health Emergen

Page Type
Product Code
Definition
The device is an acoustic wave generating extracorporeal accessory to indwelling urinary catheters intended to aid in the reduction of catheter-associated urinary tract infection (CAUTI) incidence in patients requiring long-term (= 14 days) indwelling catheterization. Intended for use during declared public health emergency.
Physical State
Battery powered driver unit and vibration actuator connected to an indwelling urological catheter.
Technical Method
To deliver acoustic waves to reduce bacterial attachment on the inner and outer surfaces of the indwelling urinary catheter.
Target Area
Intraurethral mucosal tissue surrounding, and inner and outer surfaces of an indwelling catheter.
Review Panel
Gastroenterology and Urology
Submission Type
Enforcement Discretion
Device Classification
N
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

As product code QMK is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.