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Prothia USA, Inc.

5 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
UNIVERSAL INSTRU. SET FOR NEUROVASCULAR (K831071)Prothia USA, Inc.1983-06-08
AMPLIGREFFE (K830993)Prothia USA, Inc.1983-05-03
ELPHA 500 (K823581)Prothia USA, Inc.1983-03-24
MYOGRAPH 2000 (K830058)Prothia USA, Inc.1983-03-07
MYOTEST NERVE STIMULATOR (K823583)Prothia USA, Inc.1982-12-30

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Every clearance here is in the API, with alerts when new ones post.