FDA Product Code
FDA Product Code KDW — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Pathology
- 21 CFR Citation
- 864.3250
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K970580 | SASI-DC1TS | Substance Abuse Specialties, Inc. | 1997-04-17 | Traditional | PDF ↗ |
| K951122 | CAPITOL URINE DRUG SCREEN COLLECTION KIT | Harry A. Schlakman | 1995-05-05 | Traditional | PDF ↗ |
| K931474 | DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS | Gbf Medical Group | 1994-05-10 | Traditional | PDF ↗ |
| K913967 | DOX TAMPERPROOF SPECIMEN CONTAINER SYSTEM | Doxtech, Inc. | 1991-10-18 | Traditional | PDF ↗ |
Product code KDW · Class I · Pathology. Data: openFDA.