510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781728Substantially Equivalent

Extube

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

K781728 is the FDA 510(k) clearance record for EXTUBE, a class I device, cleared for Analytichem International, Inc. on under FDA product code KEA (Resins, Ion-Exchange). FDA records list 2 510(k) clearances for Analytichem International, Inc., from to . As of , FDA records show no recalls naming K781728.

Clearance record

Decision date
Received
(75 days to decision)
Product code
KEA Resins, Ion-Exchange
Regulation
21 CFR 862.2230
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Analytichem International, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KEA

Trailing 12 months

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

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