CHEETAH I.V.D.S., MODEL 2002P— 510(k) K023370

Substantially Equivalent

Cheetah Medical, Inc.

FDA 510(k) clearance K023370 for CHEETAH I.V.D.S., MODEL 2002P, Substantially Equivalent on 2002-12-24. Applicant: Cheetah Medical, Inc..

Clearance details

Applicant: Cheetah Medical, Inc.
Product code: Code DQK
Advisory panel: Cardiovascular
Date received: 2002-10-08
Decision date: 2002-12-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ra'Ananna 43373, IL

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQK

product code DQK

Death: 10
Injury: 225
Malfunction: 2,123
Other: 2
Total: 2,360

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.