KENDALL BLUNT TUOHY EPIDURAL NEEDLE— 510(k) K954706

Unknown

Kendall Healthcare Products Co. Div.Of Tyco Health

FDA 510(k) clearance K954706 for KENDALL BLUNT TUOHY EPIDURAL NEEDLE, Unknown on 1996-05-30. Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health.

Clearance details

Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health
Product code: Code CAZ
Advisory panel: Anesthesiology
Date received: 1995-10-12
Decision date: 1996-05-30
Decision: Unknown
Clearance type: Traditional
Location: Mansfield, MA, US

Download summary PDF View on FDA.gov ↗

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.