510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K842921Substantially Equivalent

Rees & Ecker Dilution Fluid

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

K842921 is the FDA 510(k) clearance record for REES & ECKER DILUTION FLUID, a class I device, cleared for E K Ind., Inc. on under FDA product code GLG (Platelet Counting, Manual). FDA records list 50 510(k) clearances for E K Ind., Inc., from to . As of , FDA records show no recalls naming K842921.

Clearance record

Decision date
Received
(44 days to decision)
Product code
GLG Platelet Counting, Manual
Regulation
21 CFR 864.6160
Device class
Class I
Review panel
Hematology
Applicant
E K Ind., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GLG

Trailing 12 months

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

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