510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K972102Substantially Equivalent

Radius Push Over the Guide Wire Percutaneous Endoscopic Gastrostomy Kit

Radius Intl., Inc., Tarpon Springs FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972102 is the FDA 510(k) clearance record for RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT, a class II device, cleared for Radius Intl., Inc. on under FDA product code KNT (Tubes, Gastrointestinal (And Accessories)). FDA records list 5 510(k) clearances for Radius Intl., Inc., from to . As of , FDA records show no recalls naming K972102.

Clearance record

Decision date
Received
(233 days to decision)
Product code
KNT Tubes, Gastrointestinal (And Accessories)
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Radius Intl., Inc. 40178 u.s. 19 N., Tarpon Springs FL
510(k) summary
Summary
Third party review
No

Clearances, product code KNT

Trailing 12 months
2 clearances under product code KNT in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KNT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20261
September 20260
October 20260