Product Code: KBS FDA class 1 21 CFR 874.4420

Punch, Adenoid

Ear, Nose, Throat

An adenoid punch is a surgical instrument with a biting or cutting action used to remove or debulk adenoid tissue in the nasopharynx, commonly employed in adenoidectomy procedures for children with airway obstruction or chronic infections. It is classified as an FDA Class 1 device, the lowest risk category, subject only to general controls without premarket clearance requirements. Product code KBS 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
39
Registration Numbers
39
Unique Applicants
0
Years Active

Research product code KBS in seconds

The Research Assistant summarizes clearances, adverse event trends and regulation context for a product code — and cites every record.

Free to try · every answer cites its records

Basic Information

Product Code
KBS
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 39 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 39 registration numbers. Click on an entry to view related FDA registrations.