Heyer Schulte Corp.
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) | K792096 | 2 FR KELMAN CHAMBER MAINTAINER | FMI | 1979-11-16 | View |
| 510(k) | K790842 | SUBCUTANEOUS TISSUE EXPANDER | LCJ | 1979-08-03 | View |
| 510(k) | K780706 | LUMBAR NERVE ROOT SHIELD | 1978-09-07 | View | |
| 510(k) | K780417 | ASEPTIC TRANSFER SET | GAZ | 1978-04-18 | View |
| 510(k) | K771224 | RADOVAN SUBCUTANEOUS TISSUE EXPANDER | LCJ | 1977-10-11 | View |
| 510(k) | K760778 | T-TUBE DRAIN, ROUND | GCY | 1976-11-03 | View |
| 510(k) | K760784 | MISHLER 2 CHAMB FLUSHING VALVE,STAND | JXG | 1976-11-01 | View |
| 510(k) | K760785 | MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH | JXG | 1976-11-01 | View |
| 510(k) | K760501 | VALVE, STANDARD MODEL PUDENZE FLUSHING | JXG | 1976-08-30 | View |
No matching devices.
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