FDA Product Code
FDA Product Code KYA — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Obstetrics/Gynecology
- 21 CFR Citation
- 884.2982
510(k) Clearances — 5 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K900404 | VARICOSCREEN(TM) | Promedex, Inc. | 1990-12-07 | Traditional | PDF ↗ |
| K832989 | BREAST THERMAL ACTIVITY INDICATOR | Bcsi Laboratories, Inc. | 1984-01-17 | Traditional | PDF ↗ |
| K823245 | THERMAX; THERMAX SYSTEM | American Thermometer Company, Inc. | 1982-11-16 | Traditional | PDF ↗ |
| K821524 | CHIROPRATIC INFRA-RED CRYSTAL PAK | Dr. John D. Reid B.A., D.C. | 1982-09-08 | Traditional | PDF ↗ |
| K821049 | PARATHERM | American Thermometer Company, Inc. | 1982-04-29 | Traditional | PDF ↗ |
Product code KYA · Class I · Obstetrics/Gynecology. Data: openFDA.