EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS— 510(k) K991719

Unknown

Medimex Holfeld GmbH & Co.

FDA 510(k) clearance K991719 for EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS, Unknown on 1999-08-18. Applicant: Medimex Holfeld GmbH & Co..

Clearance details

Applicant: Medimex Holfeld GmbH & Co.
Product code: Code CAZ
Advisory panel: Anesthesiology
Date received: 1999-05-20
Decision date: 1999-08-18
Decision: Unknown
Clearance type: Traditional
Location: Salt Lake City, UT, US

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Adverse events under product code CAZ

product code CAZ

Injury: 145
Malfunction: 942
Other: 1
Total: 1,088

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.