FDA product code KAP: Curette, Nasal
KAP is the FDA product code for curette, nasal. It is a Class I device, regulated under 21 CFR 874.4420 and reviewed by the Ear, Nose and Throat panel. FDA has cleared 1 510(k) submission under KAP. The average 510(k) review took 9 days (median 9).
Classification
| Field | Value |
|---|---|
| Device name | Curette, Nasal |
| Device class | Class I |
| Regulation | 21 CFR 874.4420 |
| Review panel | EN — Ear, Nose and Throat |
| Medical specialty | Ear, Nose, Throat |
| Premarket route | 510(k) exempt |
Compare with all 510(k) review times · Search every KAP clearance
Top KAP applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Military Engineering, Inc. | 1 | 1987-07-15 |
Most recent KAP clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K872609 | Military Engineering, Inc. | CURETTE SET, ANTRUM, COAKLEY | 1987-07-15 | 9 |
Recalls for KAP devices
openFDA lists no recalls for product code KAP.
Frequently asked questions
What is FDA product code KAP?
KAP is the FDA product code for curette, nasal. It is a Class I device, regulated under 21 CFR 874.4420 and reviewed by the Ear, Nose and Throat panel.
What device class is KAP?
Class I, regulation 21 CFR 874.4420. Typical premarket route: 510(k) exempt.
How long does a 510(k) take for product code KAP?
Across 1 cleared submissions the average was 9 days from receipt to decision (median 9).
Which companies have the most KAP clearances?
Military Engineering, Inc. (1).
Next steps
- Run an FDA pathway report with predicate devices for product code KAP
- Run a recall and safety report across every KAP manufacturer
- Watch product code KAP for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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