
Biotronik, Inc.
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NANOS, PIKOS 01/E01, 01-A, E01-B, LP 01/LP E01 is an FDA 510(k)-cleared medical device (K952328) manufactured by Biotronik, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 28, 1995. Regulation: 8.

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