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JustGoDeep

10/22/17 8:28 PM

#114728 RE: stockdarockk #114727

First off that is chump change in the scheme of things and second they only need to sell 60,000 per quarter anywhere in the world and they breakeven, and third the MoNsTeR can't be stopped!!

Just a matter of time,

and soon enough for me!!~

srinsocal

10/22/17 11:37 PM

#114734 RE: stockdarockk #114727

2/3/2017 was Extremely Relevant, ActiPatch, First and Only Device based on PEMF (SWT) technology to gain FDA OTC Clearance.

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K152432

10/13/2015 was very relevant, ActiPatch FDA Product Category Reclassified from Class 3, the most strictly regulated, to Class 2. This Reclassification made the 2/3/2017 OTC Clearance possible.

https://www.federalregister.gov/documents/2015/10/13/2015-25923/physical-medicine-devices-reclassification-of-shortwave-diathermy-for-all-other-uses-henceforth-to

8/8/2002 was relevant, Actiband, the first generation of the ActiPatch, received FDA Clearance for "For the treatment of edema following Blepharoplasty"

https://www.accessdata.fda.gov/cdrh_docs/pdf2/K022404.pdf