510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913587Substantially Equivalent

Jtech 50 Series Cutting Loop

J-Tech, Inc., Midvale UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913587 is the FDA 510(k) clearance record for JTECH 50 SERIES CUTTING LOOP, a class II device, cleared for J-Tech, Inc. on under FDA product code FJL (Resectoscope). FDA records list 5 510(k) clearances for J-Tech, Inc., from to . As of , FDA records show no recalls naming K913587.

Clearance record

Decision date
Received
(72 days to decision)
Product code
FJL Resectoscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
J-Tech, Inc. 553 Cobblestone Dr., Midvale UT
510(k) summary
Statement
Third party review
No

Clearances, product code FJL

Trailing 12 months

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

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