Last synced on 11 April 2025 at 11:05 pm

Apparatus, Suction, Operating-Room, Wall Vacuum Powered (Export Only)

Page Type
Product Code
Definition
Intended to be used for the removal of prosthetic breast implant specimens.
Physical State
The device is a sterile, transparent, rigid bi-conical device that, when assembled, will attach to an external vacuum source and provide suction in order to remove prosthetic breast implants. This is a single use device available by prescription only, for professional use in a clinical setting. The two cones (top and bottom) are made of molded thermoplastic and seal together with a silicone O-ring.
Technical Method
The device is intended to be used for the removal of prosthetic breast implant specimens, including intact and ruptured silicone gel implants as well as intact saline implants.
Target Area
Breast
Review Panel
General and Plastic Surgery
Submission Type
Contact ODE
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 QOJ is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.

Apparatus, Suction, Operating-Room, Wall Vacuum Powered (Export Only)

Page Type
Product Code
Definition
Intended to be used for the removal of prosthetic breast implant specimens.
Physical State
The device is a sterile, transparent, rigid bi-conical device that, when assembled, will attach to an external vacuum source and provide suction in order to remove prosthetic breast implants. This is a single use device available by prescription only, for professional use in a clinical setting. The two cones (top and bottom) are made of molded thermoplastic and seal together with a silicone O-ring.
Technical Method
The device is intended to be used for the removal of prosthetic breast implant specimens, including intact and ruptured silicone gel implants as well as intact saline implants.
Target Area
Breast
Review Panel
General and Plastic Surgery
Submission Type
Contact ODE
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 QOJ is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.