Culture Kits, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K911846 | URI-THREE(TM), MODIFICATION | JXA | 1991-10-04 | View |
| 510(k) | K854672 | CANDI-KIT TM | JSI | 1986-07-11 | View |
| 510(k) | K853488 | STAPH KIT | JSI | 1985-08-28 | View |
| 510(k) | K851225 | URINE DUO | JTZ | 1985-08-13 | View |
| 510(k) | K852582 | GONI-KIT | JSX | 1985-07-12 | View |
| 510(k) | K852480 | DERM-KIT | JSI | 1985-07-09 | View |
| 510(k) | K851518 | MUELLER HINTON SENSITIVITY PLATE | JTZ | 1985-04-29 | View |
| 510(k) | K850765 | STREP-KIT | JSJ | 1985-04-24 | View |
| 510(k) | K850998 | URI-KIT | JSG | 1985-04-01 | View |
No matching devices.
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