Product Code: KAS FDA class 1 21 CFR 874.4420

Knife, Nasal

Ear, Nose, Throat

A nasal knife is a fine-bladed surgical cutting instrument used in ear, nose, and throat surgery to incise soft tissue or cartilage within the nasal cavity during procedures such as septoplasty or turbinate reduction. Classified as FDA Class 1, it is subject only to general controls and does not require premarket clearance. Product code KAS is regulated under 21 CFR 874.4420 in the Ear, Nose, Throat medical specialty. No special flags apply to this device.

510(k)s
1
FEI Numbers
79
Registration Numbers
79
Unique Applicants
1
Years Active

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Basic Information

Product Code
KAS
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 1 510(k) clearance via K numbers.

K Number Device Name
K781837 WOUND SPAN BRIDGE III

FEI Numbers

This FDA classification entry is associated with 79 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 79 registration numbers. Click on an entry to view related FDA registrations.