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Pneumotachometer
FDA product code JAX · Class 2 · Anesthesiology
104
Registered devices
2
Adverse events
1
Recalls
8
510(k) clearances
Devices with this code
N/A — HANS RUDOLPH, INC.n/a — HANS RUDOLPH, INC.n/a — HANS RUDOLPH, INC.FloSense — S D I DIAGNOSTICS INCn/a — HANS RUDOLPH, INC.N/A — HANS RUDOLPH, INC.N/A — HANS RUDOLPH, INC.FloSense — S D I DIAGNOSTICS INCFloSense — S D I DIAGNOSTICS INCn/a — HANS RUDOLPH, INC.MGC Diagnostics — MEDICAL GRAPHICS CORPORATIONN/A — HANS RUDOLPH, INC.n/a — HANS RUDOLPH, INC.n/a — HANS RUDOLPH, INC.n/a — HANS RUDOLPH, INC.N/A — HANS RUDOLPH, INC.n/a — HANS RUDOLPH, INC.FloSense — S D I DIAGNOSTICS INCn/a — HANS RUDOLPH, INC.8311 PNT — HANS RUDOLPH, INC.n/a — HANS RUDOLPH, INC.N/A — HANS RUDOLPH, INC.N/A — HANS RUDOLPH, INC.N/A — HANS RUDOLPH, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-01-09 | Philips Medical Systems (Cleveland) Inc | When the Extended Display Firled ov View reconstruction is used, the CT numbers and anatomy in teh extended region are not accurate. |
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