fda
1 records
FDA Device Recall: Ondamed Biofeedback Device, Model No. 001-00-0101 The product is a battery po
2018-05-16
Class II — The firm was marketing the Ondamed System in the US without marketing clearance. As a corrective action, the firm revised its device design to comply with regulations. The firm has notified...
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ny_corps
1 records
NY Corp: ONDAMED INC.
2002-02-22
DOMESTIC BUSINESS CORPORATION | County: Orange | Jurisdiction: New York
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