Biologics Intl., 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) | K882229 | AIR BED & FLOTATION DERMAGARD 800 & 900 SYSTEMS | IOQ | 1988-08-16 | View |
| 510(k) | K823353 | CARCINO-CEK | JJX | 1982-12-14 | View |
| 510(k) | K812060 | BI-ASO SLIDE TEST | GTQ | 1981-08-13 | View |
| 510(k) | K811375 | BI-RA SLIDE TEST | DHR | 1981-06-12 | View |
| 510(k) | K811374 | BI-CRP LATEX TEST | DCN | 1981-06-12 | View |
| 510(k) | K800605 | ANA LATEX SLIDE TEST | DHC | 1980-04-02 | View |
| 510(k) | K791609 | BE-SURE | JHJ | 1979-10-02 | View |
| 510(k) | K791607 | BETA-CELL | JSG | 1979-09-24 | View |
| 510(k) | K790898 | PREG-TEX | JHJ | 1979-07-30 | View |
No matching devices.
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