COMPRESSAR UNIVERSAL (TM) SYSTEM— 510(k) K925809

Substantially Equivalent

Instromedix, Inc.

FDA 510(k) clearance K925809 for COMPRESSAR UNIVERSAL (TM) SYSTEM, Substantially Equivalent on 1993-02-22. Applicant: Instromedix, Inc..

Clearance details

Applicant: Instromedix, Inc.
Product code: Code DXC
Advisory panel: Cardiovascular
Date received: 1992-11-17
Decision date: 1993-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hillsboro, OR, US

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Adverse events under product code DXC

product code DXC

Death: 14
Injury: 442
Malfunction: 2,209
Other: 1
Total: 2,666

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.