510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K822436Substantially Equivalent

DNA Medical Duracath

Moorehead Hospital Products, Inc., NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K822436 is the FDA 510(k) clearance record for DNA MEDICAL DURACATH, a class II device, cleared for Moorehead Hospital Products, Inc. on under FDA product code BSO (Catheter, Conduction, Anesthetic). FDA records list one 510(k) clearance for Moorehead Hospital Products, Inc. As of , FDA records show no recalls naming K822436.

Clearance record

Decision date
Received
(70 days to decision)
Product code
BSO Catheter, Conduction, Anesthetic
Regulation
21 CFR 868.5120
Device class
Class II
Review panel
Anesthesiology
Applicant
Moorehead Hospital Products, Inc.
Third party review
No

Clearances, product code BSO

Trailing 12 months

FDA records hold no clearances under product code BSO in the trailing twelve months.

FDA records show no clearances under product code BSO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BSO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260