Pennwalt Corp.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K833241 | INTREX | EAP | 1983-10-28 | View |
| 510(k) | K801860 | S.S. WHITE-PENNWALT RENEW CALCIUM HYDROX | EJK | 1980-10-10 | View |
| 510(k) | K801274 | S.S. WHITE-PENNWALT PRELUDE PIT SEALANT | EBC | 1980-06-09 | View |
| 510(k) | K800133 | PANOREX II DENTAL X-RAY UNIT | EHD | 1980-03-03 | View |
| 510(k) | K800063 | XR-710 | EAP | 1980-03-03 | View |
| 510(k) | K780981 | PORTABLE PNEUMATIC CALIBRATOR 65-150 | BXX | 1978-08-02 | View |
No matching devices.
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