fda
1 records
FDA Device Recall: XTRAC Excimer Laser, Model No. AL8000, AL10000 The intended use is targeted U
2017-04-05
Class II — When the Liquid Guide ( LLG) is not used according to the operator manual, the switch control wires may become loose and shorted. Shorted wires may lead to unintentional laser firing.
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ny_corps
1 records
NY Corp: STRATA SKIN SCIENCES, INC.
1997-12-03
FOREIGN BUSINESS CORPORATION | County: Westchester | Jurisdiction: Delaware
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SEC EDGAR
1 records
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