FDA 510(k) Applications Submitted by ADAM SPENCE CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K955111 | 11/08/1995 | MAXI-TORQUE PLUS ANGIOGRAPHIC CATHETER | ADAM SPENCE CORP. |
| K983940 | 11/05/1998 | EZ-INTRO PERCUTANEOUS CATHETER SHEATH, EZ-INTRO VESSEL DILATOR | ADAM SPENCE CORP. |
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