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Percussor, Powered-Electric
FDA product code BYI · Class 2 · Anesthesiology
981
Registered devices
282
Adverse events
3
Recalls
58
510(k) clearances
Devices with this code
inCourage® — Respiratory Technologies, Inc.SmartVest — ELECTROMED, INC.inCourage® — Respiratory Technologies, Inc.The Vest®System — HILL-ROM SERVICES PTE. LTD.ClearChest® — Respiratory Technologies, Inc.G5® — GENERAL PHYSIOTHERAPY INCAffloVest — Tactile Systems Technology, Inc.inCourage® — Respiratory Technologies, Inc.The Vest®System — HILL-ROM SERVICES PTE. LTD.inCourage® — Respiratory Technologies, Inc.G5® — GENERAL PHYSIOTHERAPY INCinCourage® — Respiratory Technologies, Inc.G5® — GENERAL PHYSIOTHERAPY INCG5® — GENERAL PHYSIOTHERAPY INCVIBRALUNG® — WESTMED, INC.G5® — GENERAL PHYSIOTHERAPY INCinCourage® — Respiratory Technologies, Inc.G5® — GENERAL PHYSIOTHERAPY INCG5® — GENERAL PHYSIOTHERAPY INCThe Vest®System — HILL-ROM SERVICES PTE. LTD.SmartVest — ELECTROMED, INC.G5® — GENERAL PHYSIOTHERAPY INCG5® — GENERAL PHYSIOTHERAPY INCClearChest® — Respiratory Technologies, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-03-31 | Smiths Medical ASD Inc. | The firm became aware via complaints that one lot of ACE MDI Spacers with Small Masks and one lot of Palm Cups (Large) may have incorrect shipping box labels. |
| 2017-09-15 | HILL-ROM MANUFACTURING, INC. | Monarch Electromagnetic Interference (EMI) may disrupt the operation of implanted pacemakers or implantable cardioverter defibrillators as well as other devices |
| 2014-11-13 | Aptalis Pharmatech Inc. | Customer notification that the device may be difficult to open or close. |
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