FDA Product Code
FDA Product Code LRD — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Ear, Nose, Throat
- 21 CFR Citation
- 874.5220
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K984345 | AROMAPATCH | Envis, Inc. | 1999-03-19 | Traditional | PDF ↗ |
| K932522 | AMSCO STERILE RECOVERIES SURGICAL PACKS | Amsco Sterile Recoveries, Inc. | 1994-09-09 | Traditional | PDF ↗ |
| K942789 | MISTASSIST | The Merlin Corp. | 1994-08-12 | Traditional | PDF ↗ |
| K940133 | THE EXPANDACELL EAR PACK | Denver Splint Co. | 1994-05-23 | Traditional | PDF ↗ |
| K925022 | SURGICAL TRAY (STERILE) | Customed, Inc. | 1993-04-26 | Traditional | PDF ↗ |
| K920842 | AEROSOL DELIVERY SYSTEMS | Hospitak, Inc. | 1992-05-15 | Traditional | PDF ↗ |
Product code LRD · Class I · Ear, Nose, Throat. Data: openFDA.