510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K880850Substantially Equivalent

Keith Nasogastric Sump Tube W/anti-Reflux Valve

Kmb Medical Products Co., Hazelwood MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880850 is the FDA 510(k) clearance record for KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE, a class II device, cleared for Kmb Medical Products Co. on under FDA product code FEG (Tube, Double Lumen For Intestinal Decompression And/Or Intubation). FDA records list one 510(k) clearance for Kmb Medical Products Co. As of , FDA records show 2 recalls naming K880850.

Clearance record

Decision date
Received
(86 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
Kmb Medical Products Co. 320 Brookes Dr., Suite 110, Hazelwood MO
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