510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781751Substantially Equivalent

Catheter, Akron Foley Teflon

Latex Ind., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K781751 is the FDA 510(k) clearance record for CATHETER, AKRON FOLEY TEFLON, a class II device, cleared for Latex Ind., Inc. on under FDA product code KOD (Catheter, Urological). FDA records list 14 510(k) clearances for Latex Ind., Inc., from to . As of , FDA records show no recalls naming K781751.

Clearance record

Decision date
Received
(98 days to decision)
Product code
KOD Catheter, Urological
Regulation
21 CFR 876.5130
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Latex Ind., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KOD

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