FDA 510(k) Applications Submitted by HEART TECHNOLOGY MFG., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960379 | 01/26/1996 | ROTABLATOR SYSTEM'S GUIDE WIRE LINE: SUPPORT ROTAWIRE RAIL ROTA WIRE | HEART TECHNOLOGY MFG., INC. |
| K954604 | 10/04/1995 | ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM ROTABLATOR SYSTEM'S GUIDE WIRE LINE; HTI FLOPPY | HEART TECHNOLOGY MFG., INC. |
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