OMNIGRAPH 6000— 510(k) K880357

Substantially Equivalent

Telemed Div.

FDA 510(k) clearance K880357 for OMNIGRAPH 6000, Substantially Equivalent on 1988-08-02. Applicant: Telemed Div..

Clearance details

Applicant: Telemed Div.
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 1988-01-28
Decision date: 1988-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hoffman Estates, IL, 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.