HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE— 510(k) K903523

Substantially Equivalent

Hewlett-Packard Co.

FDA 510(k) clearance K903523 for HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE, Substantially Equivalent on 1990-10-23. Applicant: Hewlett-Packard Co..

Clearance details

Applicant: Hewlett-Packard Co.
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 1990-08-06
Decision date: 1990-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Germany, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQA

product code DQA

Death: 66
Malfunction: 2,867
Other: 1
Total: 2,934

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.