SIRECUST 1280/1281 & 960/961 PATIENT MONITORS— 510(k) K881939

Name: FDA 510(k) clearance K881939
Creator: U.S. Food and Drug Administration
Published: 1988-07-18

Substantially Equivalent

Siemens Medical Electronics

FDA 510(k) clearance K881939 for SIRECUST 1280/1281 & 960/961 PATIENT MONITORS, Substantially Equivalent on 1988-07-18. Applicant: Siemens Medical Electronics. Device class: 2.

Clearance details

Applicant: Siemens Medical Electronics
Product code: Code DPS
Device class: Class 2
Regulation: 21 CFR 870.2340
Advisory panel: Cardiovascular
Date received: 1988-05-09
Decision date: 1988-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danvers, MA, US

Download summary PDF View on FDA.gov ↗

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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.