510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K183508Unknown

Micro Transgastric-Jejunal Feeding Device

Applied Medical Technology Inc, Brecksville OH / Traditional, Unknown
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K183508 is the FDA 510(k) clearance record for Micro Transgastric-Jejunal Feeding Device, a class II device, cleared for Applied Medical Technology, Inc. on under FDA product code KNT (Tubes, Gastrointestinal (And Accessories)). FDA records list 25 510(k) clearances for Applied Medical Technology, Inc., from to . As of , FDA records show no recalls naming K183508.

Clearance record

Decision date
Received
(101 days to decision)
Product code
KNT Tubes, Gastrointestinal (And Accessories)
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Applied Medical Technology, Inc. 8006 Katherine Blvd., Brecksville OH
510(k) summary
Summary PDF
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