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Re: JustGoDeep post# 235510

Wednesday, 09/16/2020 11:44:35 PM

Wednesday, September 16, 2020 11:44:35 PM

Post# of 330562
huh? here is what the fda said

The Food and Drug Administration (FDA) is proposing to reclassify the shortwave diathermy (SWD) for all other uses, a preamendments class III device, into class II (special controls), and to rename the device “nonthermal shortwave therapy (SWT).” FDA is proposing this reclassification on its own initiative based on new information. FDA is also proposing a technical correction in the regulation for the carrier frequency for SWD and nonthermal SWT devices. This proposed action would implement certain regulatory requirements.

nothing about any error, simple administrative reclassification

THEY HATE ME CAUSE THEY AINT ME

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