fda
1 records
FDA Device Recall: lnvatec SpA brand Diver C.E., Model/Catalog Numbers: DVR010014145, DVR011014145
2013-06-12
Class II — Devices labeled for an intended use was not included in the existing 510(k) or PMA, in that, the Indications for use was modified.
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ny_corps
1 records
NY Corp: INVATEC, LTD.
2007-06-19
FOREIGN LIMITED PARTNERSHIP | County: New York | Jurisdiction: Texas
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