FDA Product Code
FDA Product Code KMO — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- General Hospital
- 21 CFR Citation
- 880.5160
510(k) Clearances — 5 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K921852 | 4 SURE TM RECTAL TUBE | Boston Pacific Medical, Inc. | 1993-10-08 | Traditional | PDF ↗ |
| K893809 | COUGH PILLOW | Custom Hospitals Products | 1989-08-28 | Traditional | PDF ↗ |
| K883214 | THORACIC SUPPORT SYSTEM | Storer Medical Products | 1989-01-17 | Traditional | PDF ↗ |
| K882592 | HEART HUGGER STERNUM SUPPORT HARNESS | General Cardiac Technology, Inc. | 1988-09-20 | Traditional | PDF ↗ |
| K792629 | STERILIZATION PROCESS/T-BINDER | Procter & Gamble Mfg. Co. | 1980-01-11 | Traditional | PDF ↗ |
Product code KMO · Class I · General Hospital. Data: openFDA.