CURITY CALIBRATED TUOHY TYPE EPIDURAL NEEDLE— 510(k) K921288

Clearance details

Applicant

Kendall Healthcare Products Co. Div.Of Tyco Health

Product code

Code BSP

Device class

Class 2

Regulation

21 CFR 868.5150

Advisory panel

Anesthesiology

Date received

1992-03-17

Decision date

1993-01-27

Decision

Substantially Equivalent

Clearance type

Traditional

Location

Mansfield, MA, US

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• K973763 — KENDALL CURITY IODOFORM PACKING STRIP1997-12-31
• K973511 — KENDALL CURITY PETROLATUM GAUZE1997-12-16
• K973507 — KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)1997-12-15
• K973619 — KENDALL CURITY NON-ADHERING DRESSING1997-12-10
• K973509 — KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING1997-12-04

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 →