510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K011759Substantially Equivalent

Radius Next Generation Guidewire

Radius Medical Technologies, Inc., Maynard MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K011759 is the FDA 510(k) clearance record for RADIUS NEXT GENERATION GUIDEWIRE, a class II device, cleared for Radius Medical Technologies, Inc. on under FDA product code OCY (Endoscopic Guidewire, Gastroenterology-Urology). FDA's definition for product code OCY reads: "To provide access to gi or gu tract for the purpose of passing or exchanging other accessories". FDA records list 9 510(k) clearances for Radius Medical Technologies, Inc., from to . As of , FDA records show no recalls naming K011759.

Clearance record

Decision date
Received
(78 days to decision)
Product code
OCY Endoscopic Guidewire, Gastroenterology-Urology
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Radius Medical Technologies, Inc. 63 Great Rd., Maynard MA
510(k) summary
Summary
Third party review
No

Clearances, product code OCY

Trailing 12 months

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

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