FDA 510(k) Applications Submitted by MAYLIN TRUESDELL
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K150235 |
02/02/2015 |
CLEARSIGN II Amplifier, 40 channels, CLEARSIGN II Amplifier, 80 channels, CLEARSIGN II Amplifier, 120 channels, CLEARSIGN II Amplifer, 160 channels |
BOSTON SCIENTIFIC CORPORATION |
K180734 |
03/20/2018 |
SmartLinx Vitals Plus Patient Monitoring System |
Capsule Technologie |
K152693 |
09/21/2015 |
CLEARSIGN II Amplifier 40 Channels, CLEARSIGN II Amplifier 80 Channels, CLEARSIGN II Amplifier 120 Channels, CLEARSIGN II Amplifier 160 Channels |
BOSTON SCIENTIFIC CORPORATION |
K133566 |
11/20/2013 |
ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM WITH THE PERIPHERAL ROTALINK PLUS |
BOSTON SCIENTIFIC CORP. |
K183638 |
12/26/2018 |
SmartLinx Vitals Plus Patient Monitoring System |
Capsule Technologie |
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