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Esophageal Protection Device For Use In Percutaneous Cardiac Catheter Ablation Procedures, Mechanical Deviation

Page Type
Product Code
Definition
This device is placed in the lumen of the esophagus to reduce the likelihood of esophageal injury or a specific adverse event during cardiac ablation procedures. The device uses mechanical means to deviate the esophagus away from the source of ablation energy
Physical State
A long component that allows for insertion into the esophagus and for movement of the esophagus. The device may include a handle to allow for operator control of deviation.
Technical Method
Uses a mechanism inserted into the esophagus to move the esophagus away from the heart.
Target Area
Esophagus
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.5710
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

Product code QXU is linked to regulation 21CFR870.5710, which does not seem to exist yet. It may be pending at the moment.

Esophageal Protection Device For Use In Percutaneous Cardiac Catheter Ablation Procedures, Mechanical Deviation

Page Type
Product Code
Definition
This device is placed in the lumen of the esophagus to reduce the likelihood of esophageal injury or a specific adverse event during cardiac ablation procedures. The device uses mechanical means to deviate the esophagus away from the source of ablation energy
Physical State
A long component that allows for insertion into the esophagus and for movement of the esophagus. The device may include a handle to allow for operator control of deviation.
Technical Method
Uses a mechanism inserted into the esophagus to move the esophagus away from the heart.
Target Area
Esophagus
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.5710
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

Product code QXU is linked to regulation 21CFR870.5710, which does not seem to exist yet. It may be pending at the moment.