510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960176Substantially Equivalent

Davol Nasogastric Sump Tube W/prevent Filter

C.R. Bard Inc, Canston RI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960176 is the FDA 510(k) clearance record for DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER, a class II device, cleared for C.R. Bard, Inc. on under FDA product code FEG (Tube, Double Lumen For Intestinal Decompression And/Or Intubation). FDA records list 646 510(k) clearances for C.R. Bard, Inc., from to . As of , FDA records show 17 recalls naming K960176.

Clearance record

Decision date
Received
(190 days to decision)
Product code
FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
C.R. Bard, Inc. 100 Sockanossett Crossroad, Canston RI
510(k) summary
Summary
Third party review
No

Clearances, product code FEG

Trailing 12 months

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

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