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
K930510Substantially Equivalent

Radius Enteral Feeding Tube

Radius Intl., Inc., Grayslake IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930510 is the FDA 510(k) clearance record for RADIUS ENTERAL FEEDING TUBE, a class II device, cleared for Radius Intl., Inc. on under FDA product code BSS (Tube, Nasogastric). FDA records list 5 510(k) clearances for Radius Intl., Inc., from to . As of , FDA records show no recalls naming K930510.

Clearance record

Decision date
Received
(730 days to decision)
Product code
BSS Tube, Nasogastric
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Radius Intl., Inc. 21860 W. Washington St., Grayslake IL
510(k) summary
Summary
Third party review
No

Clearances, product code BSS

Trailing 12 months

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

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