510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K915439Unknown

Nasogastric Feeding Tube Kits

Sandoz Nutrition, Minneapolis MN / Traditional, Unknown
FDA source (opens on fda.gov)

K915439 is the FDA 510(k) clearance record for NASOGASTRIC FEEDING TUBE KITS, a class II device, cleared for Sandoz Nutrition on under FDA product code FPD (Tube, Feeding). FDA records list 20 510(k) clearances for Sandoz Nutrition, from to . As of , FDA records show one recall naming K915439.

Clearance record

Decision date
Received
(85 days to decision)
Product code
FPD Tube, Feeding
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Sandoz Nutrition 5320 W. Twenty Third St., Minneapolis MN
510(k) summary
Statement
Third party review
No

Clearances, product code FPD

Trailing 12 months

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

FDA records show no clearances under product code FPD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FPD, 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