KCJ — Applicator, Ent Class I
FDA product code KCJ covers "Applicator, 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
- KCJ
- 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 |
|---|---|---|---|
| K923679 | ethicon endo-surgery | ENDOPATH TISSUE RETAINING COMPONENT | September 9, 1992 |
| K921053 | laparomed | LAPAROMED LIGATING LOOP | August 6, 1992 |
| K894369 | apdyne medical | APDYNE PHENOL APPLICATOR KIT | October 12, 1989 |
| K832667 | kells medical | LUCAE'S EAR & NASAL APPLICATORS | September 29, 1983 |