CARDIO-SLIDECOMP— 510(k) K790869

Substantially Equivalent

Creative Instruments

FDA 510(k) clearance K790869 for CARDIO-SLIDECOMP, Substantially Equivalent on 1979-05-17. Applicant: Creative Instruments.

Clearance details

Applicant: Creative Instruments
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 1979-05-07
Decision date: 1979-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.