SIEMENS SIRECUST 730 PATIENT MONITOR— 510(k) K890791

Substantially Equivalent

Siemens Medical Electronics

FDA 510(k) clearance K890791 for SIEMENS SIRECUST 730 PATIENT MONITOR, Substantially Equivalent on 1989-05-02. Applicant: Siemens Medical Electronics.

Clearance details

Applicant: Siemens Medical Electronics
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 1989-02-17
Decision date: 1989-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danvers, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.