LOPER CELIAC PLEXUS BLOCK CATHETER KIT— 510(k) K895955

Substantially Equivalent

Opticon Medical, Inc.

FDA 510(k) clearance K895955 for LOPER CELIAC PLEXUS BLOCK CATHETER KIT, Substantially Equivalent on 1990-02-22. Applicant: Opticon Medical, Inc..

Clearance details

Applicant: Opticon Medical, Inc.
Product code: Code CAZ
Advisory panel: Anesthesiology
Date received: 1989-10-11
Decision date: 1990-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gurnee, IL, 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.