Home › Device types › FWF
Camera, Television, Endoscopic, Without Audio
FDA product code FWF · Class 1 · General, Plastic Surgery
119
Registered devices
290
Adverse events
2
Recalls
23
510(k) clearances
Devices with this code
N/A — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.C-Camsource® — Joimax GmbHN/A — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.C-Camsource® — Joimax GmbHHERMES — Smith & Nephew, Inc.Camsource® — Joimax GmbHNA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.Intellijet — Smith & Nephew, Inc.DCI — Karl Storz GmbH & Co. KGGimmi — Gimmi GmbHN/A — Smith & Nephew, Inc.Hayden Medical — Hayden Medical, Inc.NA — Smith & Nephew, Inc.Hayden Medical — Hayden Medical, Inc.Camsource® — Joimax GmbHPROCAM Basic PAL — EclerisN/A — PENTAX OF AMERICA, INC.PROCAM — EclerisRZ Medizintechnik GmbH — RZ-Medizintechnik GmbH
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-01-19 | Smith & Nephew, Inc Endoscopy Division | Surgical camera control units were not designed and manufactured to pass the IEC 60101 testing for electrical fast transients (EFT) |
| 2007-01-19 | Smith & Nephew, Inc Endoscopy Division | Surgical camera control units were not designed and manufactured to pass the IEC 60101 testing for electrical fast transients (EFT) |
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