On the (b)(4) 2018 (b)(4) received a customer email; customer emailed itovi requesting the recall form, but also mentioned that on of her clients were shocked by the device.Email routed to (b)(4).On the (b)(4) 2018 (b)(4) received a customer email; customer claims a teenager that they scanned was shocked twice, but that she didn't think much of it.Email routed to (b)(4).Specification developer and finished product manufacturer: establishment: (b)(4).Classification name: device, galvanic skin response measurement, product code: gzo, device class: 2, regulation number: (b)(4), medical specialty: neurology, registered establishment name: itovi.(b)(4).Establishment operations: manufacturer.Complaint file establishment for specification developer and finished product manufacturer (b)(4).Status: active.Note firm may have additional establishment types.Please review listings for further information.Date of registration status: 2018.(b)(4).Specification developer and finished product manufacturer is in the process of redesigning a new medical device for subsequent replacement.
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On the (b)(4) 2018 (b)(4) received a customer email; customer emailed itovi requesting the recall form, but also mentioned that one of her clients were shocked by the device.Email routed to (b)(4).On the (b)(4) 2018 (b)(4) received a customer email; customer claims a teenager that they scanned was shocked twice, but that she didn't think much of it.Email routed to (b)(4).
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