Product Code: KBE FDA class 1 21 CFR 874.4420

Snare, Nasal

Ear, Nose, Throat

A nasal snare is a surgical instrument consisting of a wire loop that can be tightened around nasal polyps or other tissue to sever and remove them from the nasal cavity, used in outpatient or operative ENT settings. It is classified as an FDA Class 1 device, the lowest risk category, subject only to general controls without requiring premarket notification. Product code KBE is regulated under 21 CFR 874.4420 in the Ear, Nose, Throat medical specialty. No special flags apply to this device.

510(k)s
0
FEI Numbers
55
Registration Numbers
55
Unique Applicants
0
Years Active

Basic Information

Product Code
KBE
Device Class
FDA class 1
Regulation Number
874.4420
Medical Specialty
Ear, Nose, Throat
Review Panel
EN
Submission Type
4

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

FEI Numbers

This FDA classification entry is associated with 55 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 55 registration numbers. Click on an entry to view related FDA registrations.