Heart Technology Mfg., Inc.

Heart Technology Mfg., Inc. holds 3 FDA 510(k) medical device clearances, first cleared 1995, most recent 1996.

Top product codes for Heart Technology Mfg., Inc.

MCW — Cardiovascular3 devices

Recent clearances by Heart Technology Mfg., Inc.

K960379 — ROTABLATOR SYSTEM'S GUIDE WIRE LINE: SUPPORT ROTAWIRE RAIL ROTA WIRECode MCW·1996-04-25
K954604 — ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM ROTABLATOR SYSTEM'S GUIDE WIRE LINE; HTI FLOPPYCode MCW·1996-01-18
K953997 — ROTABLATOR ROTATIONAL ANGIOPLASTYCode MCW·1995-12-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.