Product Code: KBD FDA class 1 21 CFR 874.4420

Scissors, Nasal

Ear, Nose, Throat

Nasal scissors are surgical cutting instruments specifically designed for use within the nasal cavity to trim, excise, or dissect tissue such as mucosa, polyps, or septum during otolaryngological procedures. They are classified as FDA Class 1 devices, the lowest risk tier, subject only to general controls and not requiring premarket clearance. Product code KBD is regulated under 21 CFR 874.4420 in the Ear, Nose, Throat medical specialty. No special flags apply to this device.

510(k)s
3
FEI Numbers
127
Registration Numbers
127
Unique Applicants
3
Years Active
6

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Basic Information

Product Code
KBD
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

510(k) Clearance History

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Related 510(k) Clearances

This FDA classification is associated with 3 510(k) clearances via K numbers.

K Number Device Name
K851763 13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK
K822524 EAR SPOON
K791124 SURGICAL SCISSORS

FEI Numbers

This FDA classification entry is associated with 127 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 127 registration numbers. Click on an entry to view related FDA registrations.