CIRCAMED HOLTER VERSION 4— 510(k) K894956

Substantially Equivalent

Circadian, Inc.

FDA 510(k) clearance K894956 for CIRCAMED HOLTER VERSION 4, Substantially Equivalent on 1990-02-05. Applicant: Circadian, Inc..

Clearance details

Applicant: Circadian, Inc.
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 1989-08-04
Decision date: 1990-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

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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.