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Calculator, Pulmonary Function Data
FDA product code BZC · Class 2 · Anesthesiology
407
Registered devices
67
Adverse events
5
Recalls
90
510(k) clearances
Devices with this code
Jaeger — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHCOSMED — C O S M E D SRLJaeger — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHVyaire — Jaeger Medical GmbHVyaire — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHVyaire — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHInnocor — Innovision ApSJaeger — Jaeger Medical GmbHVyaire — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHVyaire — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHVyaire — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHVyaire — Jaeger Medical GmbHVyaire — Jaeger Medical GmbHJaeger — Jaeger Medical GmbHJaeger — Jaeger Medical GmbH
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-08 | Vyaire Medical, Inc. | Potential of the nozzle separating during patient use. |
| 2016-05-13 | Innovision A/S | The purpose of the recall is to replace data transmission cable (USB-cable) connecting the lnnocor device with an external computer. The replacement USB cable |
| 2009-11-19 | Philips Healthcare Inc. | Power cords' prongs may crack or fail -- Philips was notified that FDA is investigating whether certain types of Electri-Cord Manufacturing Company power cords |
| 2009-11-19 | Philips Healthcare Inc. | Power cords' prongs may crack or fail -- Philips was notified that FDA is investigating whether certain types of Electri-Cord Manufacturing Company power cords |
| 2009-11-19 | Philips Healthcare Inc. | Power cords' prongs may crack or fail -- Philips was notified that FDA is investigating whether certain types of Electri-Cord Manufacturing Company power cords |
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