CureZone   Log On   Join
Re: Nothing vague or misleading about this: ParaZapper Works! - video published 2003
 
jaguar57 Views: 1,550
Published: 5 years ago
 
This is a reply to # 2,319,568

Re: Nothing vague or misleading about this: ParaZapper Works! - video published 2003


WTF? Class III is the riskiest category, not the "best" (which you imply), and they need to be FDA approved which yours is not. This is from the FDA website:

What does it mean for FDA to "classify" a medical device?

FDA classifies medical devices based on the risks associated with the device. Devices are classified into one of three categories—Class I, Class II, and Class III.

Class I devices are deemed to be low risk and are therefore subject to the least regulatory controls. For example, dental floss is classified as Class I device.

Class II devices are higher risk devices than Class I and require greater regulatory controls to provide reasonable assurance of the device’s safety and effectiveness. For example, condoms are classified as Class II devices.

Class III devices are generally the highest risk devices and are therefore subject to the highest level of regulatory control. Class III devices must typically be approved by FDA before they are marketed. For example, replacement heart valves are classified as Class III devices.
 

 
Printer-friendly version of this page Email this message to a friend
Alert Moderators
Report Spam or bad message  Alert Moderators on This GOOD Message

This Forum message belongs to a larger discussion thread. See the complete thread below. You can reply to this message!


 

Donate to CureZone


CureZone Newsletter is distributed in partnership with https://www.netatlantic.com


Contact Us - Advertise - Stats

Copyright 1999 - 2021  curezone.com

2.938 sec, (1)