Curette, Nasal
A nasal curette is a surgical scraping instrument used in otolaryngology procedures to remove tissue from within the nasal passages, such as during the treatment of nasal polyps, hypertrophic mucosa, or other nasal conditions. It is classified as an FDA Class 1 device, the lowest risk tier, subject only to general controls without premarket clearance requirements. Product code KAP is regulated under 21 CFR 874.4420 in the Ear, Nose, Throat medical specialty. No special flags apply to this device.
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Basic Information
- Product Code
- KAP
- Device Class
- FDA class 1
- Regulation Number
- 874.4420
- Medical Specialty
- Ear, Nose, Throat
- Review Panel
- EN
- Submission Type
- 4
Device Characteristics
510(k) Clearance History
Related 510(k) Clearances
This FDA classification is associated with 1 510(k) clearance via K numbers.
| K Number | Device Name | Decision Date | Decision | Applicant |
|---|---|---|---|---|
| K872609 | CURETTE SET, ANTRUM, COAKLEY | Jul 15, 1987 | Substantially Equivalent | Military Engineering, Inc. |
FEI Numbers
This FDA classification entry is associated with 94 FEI numbers. Click on an entry to view related FDA registrations.
Registration Numbers
This FDA classification entry is associated with 94 registration numbers. Click on an entry to view related FDA registrations.