FDA Product Code
FDA Product Code KDX — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Pathology
- 21 CFR Citation
- 864.4010
510(k) Clearances — 8 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K872625 | DECALCIFYING SOLUTION | Stephens Scientific | 1987-08-06 | Traditional | PDF ↗ |
| K850636 | SIMUTANEOUS FIXATION & DECALCIFYING SOLUTION CAL-E | Fisher Scientific Co., LLC | 1985-03-20 | Traditional | PDF ↗ |
| K842726 | DECALCIFIER SOLUTION | E K Ind., Inc. | 1984-08-03 | Traditional | PDF ↗ |
| K841488 | DECALCIFIER I | Surgipath Medical Industries, Inc. | 1984-05-02 | Traditional | PDF ↗ |
| K822036 | VOLU-SOL DECALCIFER | Volu Sol Medical Industries | 1982-08-03 | Traditional | PDF ↗ |
| K821443 | FORMICAL | Lerner Laboratories, Inc. | 1982-06-02 | Traditional | PDF ↗ |
| K811801 | CAL-RITE | Richard-Allan Medical Ind., Inc. | 1981-07-28 | Traditional | PDF ↗ |
| K810836 | DECALCIFIER II | Surgipath | 1981-04-23 | Traditional | PDF ↗ |
Product code KDX · Class I · Pathology. Data: openFDA.