Bio-Dyne, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K900691 | BIODYNE INSTRUMENT WIPES | GEC | 1990-03-08 | View |
| 510(k) | K883984 | HEMORX COLD PACK | LKX | 1988-12-22 | View |
| 510(k) | K864261 | MODEL 3500 INFANT RESPIRATION & HEART RATE MONITOR | BZQ | 1987-03-27 | View |
No matching devices.
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