Last synced on 18 April 2025 at 11:05 pm

Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

Page Type
Product Code
Definition
Transurethral insert for urinary occlusion/control in women with urinary incontinence
Physical State
balloon tipped catheter, insertion device
Technical Method
A balloon tipped catheter is inserted into the urethra. Deflation or removal of the device results in fluid movement
Target Area
urethra
Review Panel
Gastroenterology and Urology
Submission Type
PMA
Device Classification
Class 3
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code OCK to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.

Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

Page Type
Product Code
Definition
Transurethral insert for urinary occlusion/control in women with urinary incontinence
Physical State
balloon tipped catheter, insertion device
Technical Method
A balloon tipped catheter is inserted into the urethra. Deflation or removal of the device results in fluid movement
Target Area
urethra
Review Panel
Gastroenterology and Urology
Submission Type
PMA
Device Classification
Class 3
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code OCK to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.