TearLab Resubmits 510(k) for U.S. FDA Clearance of the TearLab Discovery™ MMP-9 Test
TEARLAB CORP (TEAR)
Last tearlab corp earnings: 11/13 04:01 pm
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US:NASDAQ Investor Relations:
tearlab.com/investors.htm
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Source: GlobeNewswire
ESCONDIDO, Calif., April 22, 2020 (GLOBE NEWSWIRE) -- TearLab Corporation (OTCQB: TEAR) (“TearLab” or the “Company”) today announced that the U.S. Food and Drug Administration (FDA) has accepted the resubmission of its 510(k) application for the potential clearance of its TearLab Discovery™ MMP-9 Test, the Company’s next-generation in-vitro diagnostic testing system. The submission covers the TearLab Discovery™ Platform and its single-use, disposable Test Card measuring the inflammatory biomarker, matrix metalloproteinase 9 (MMP-9). TearLab Discovery™ will also be capable of performing the Company’s current FDA cleared tear osmolarity test. Seph Jensen, TearLab's Chief Executive Officer commented, “We are excited to complete the resubmission of our 510(k) application for the TearLab Discovery™ platform. We believe this next generation platform, which utilizes comprehensive in vitro diagnostic testing, will offer eye care professionals greater precision and efficiency to aid in the
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