1481 T DIGITAL TELEMETRY SYSTEM WITH S-T SEGMENT ANALYSIS OPTION— 510(k) K951371

Substantially Equivalent

Siemens Medical Solutions USA, Inc.

FDA 510(k) clearance K951371 for 1481 T DIGITAL TELEMETRY SYSTEM WITH S-T SEGMENT ANALYSIS OPTION, Substantially Equivalent on 1995-10-04. Applicant: Siemens Medical Solutions USA, Inc..

Clearance details

Applicant
Siemens Medical Solutions USA, Inc.
Product code
Code DSI
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Danvers, MA, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code DSI

product code DSI
Death
170
Injury
729
Malfunction
10,680
Total
11,579

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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