510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K990765Substantially Equivalent

Flexfinder Guide Wire(regular Shaft/stiff Shaft) Marked Ink Bands, Flexfinder Guide Wire (Regular Shaft/stiff Shaft) No

Flexmedics, Minnetonka MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K990765 is the FDA 510(k) clearance record for FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER GUIDE WIRE (REGULAR SHAFT/STIFF SHAFT) NO, a class II device, cleared for Flexmedics 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 20 510(k) clearances for Flexmedics, from to . As of , FDA records show no recalls naming K990765.

Clearance record

Decision date
Received
(7 days to decision)
Product code
OCY Endoscopic Guidewire, Gastroenterology-Urology
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Flexmedics 12400 Whitewater Dr., Suite 2040, Minnetonka MN
510(k) summary
Statement
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