ESPOCAN COMBINED SPINAL/EPIDURAL NEEDLE SET & TRAY— 510(k) K932400

Unknown

B. Braun of America, Inc.

FDA 510(k) clearance K932400 for ESPOCAN COMBINED SPINAL/EPIDURAL NEEDLE SET & TRAY, Unknown on 1993-12-13. Applicant: B. Braun of America, Inc..

Clearance details

Applicant: B. Braun of America, Inc.
Product code: Code BSP
Advisory panel: Anesthesiology
Date received: 1993-05-18
Decision date: 1993-12-13
Decision: Unknown
Clearance type: Traditional
Location: Bethlehem, PA, US

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Adverse events under product code BSP

product code BSP

Death: 2
Total: 2

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.