
Meadox Medicals, Div. Boston Scientific Corp.
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NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER is an FDA 510(k)-cleared medical device (K952887) manufactured by Meadox Medicals, Div. Boston Scientific Corp.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on August 17, 1995.

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