Konigsberg Instruments, 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) | K980980 | MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50 | FFX | 1998-06-15 | View |
| 510(k) | K813331 | P51 ANGIOPLASTY PRESSURE TRANSDUCER | LIT | 1981-12-29 | View |
| 510(k) | K811083 | ESOPHAGEAL MOTILITY PROBE | FFT | 1981-08-13 | View |
No matching devices.
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