KCP — Syringe, Ent Class I
FDA product code KCP covers "Syringe, Ent", a Class I medical device regulated under 21 CFR 874.5220. Submissions are reviewed by the Ear, Nose, Throat panel. At least 4 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- KCP
- Device Class
- Class I
- Regulation Number
- 874.5220
- Submission Type
- Review Panel
- EN
- Medical Specialty
- Ear, Nose, Throat
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K840311 | imm enterprises | CAT. 7-EAR, NOSE & THROAT DEVICES | May 9, 1984 |
| K822754 | american hospital supply | EAR/ULCER SYRINGE | October 4, 1982 |
| K810284 | r. wolf medical instruments | AUTOMATIC TEFLON INJECTION SYRINGE | March 11, 1981 |
| K780599 | abco dealers | SYRINGE, EAR & ULCER | April 19, 1978 |