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Optovent AB

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K003704 OPTOVENT RESPONS, OPTOVENT RENEE (OPTOVENT RESPONS WITHOUT PULSE OXIMETRY MODULE)BZQ2001-02-05 View
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