LRD — Applicator, Ent Drug Class I
FDA Device Classification
Classification Details
- Product Code
- LRD
- 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 |
|---|
| K984345 | envis | AROMAPATCH | March 19, 1999 |
| K932522 | amsco sterile recoveries | AMSCO STERILE RECOVERIES SURGICAL PACKS | September 9, 1994 |
| K942789 | merlin | MISTASSIST | August 12, 1994 |
| K940133 | denver splint | THE EXPANDACELL EAR PACK | May 23, 1994 |
| K925022 | customed | SURGICAL TRAY (STERILE) | April 26, 1993 |
| K920842 | hospitak | AEROSOL DELIVERY SYSTEMS | May 15, 1992 |