510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K893888Substantially Equivalent

Hollister Feeding Tube Attachment Device

Hollister, Inc., Libertyville IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893888 is the FDA 510(k) clearance record for HOLLISTER FEEDING TUBE ATTACHMENT DEVICE, a class II device, cleared for Hollister, Inc. on under FDA product code KNT (Tubes, Gastrointestinal (And Accessories)). FDA records list 85 510(k) clearances for Hollister, Inc., from to . As of , FDA records show no recalls naming K893888.

Clearance record

Decision date
Received
(140 days to decision)
Product code
KNT Tubes, Gastrointestinal (And Accessories)
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Hollister, Inc. 2000 Hollister Dr., Libertyville IL
Third party review
No

Clearances, product code KNT

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