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Heart Technology Mfg., Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K960379 ROTABLATOR SYSTEM'S GUIDE WIRE LINE: SUPPORT ROTAWIRE RAIL ROTA WIREMCW1996-04-25 View
510(k) K954604 ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM ROTABLATOR SYSTEM'S GUIDE WIRE LINE; HTI FLOPPYMCW1996-01-18 View
510(k) K953997 ROTABLATOR ROTATIONAL ANGIOPLASTYMCW1995-12-22 View
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