510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K891175Substantially Equivalent

Edl Abnormal Coagulation Control

Elite Diagnostic, Ltd., Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K891175 is the FDA 510(k) clearance record for EDL ABNORMAL COAGULATION CONTROL, a class II device, cleared for Elite Diagnostic , Ltd. on under FDA product code GGL (Control, White-Cell). FDA records list 5 510(k) clearances for Elite Diagnostic , Ltd., from to . As of , FDA records show no recalls naming K891175.

Clearance record

Decision date
Received
(35 days to decision)
Product code
GGL Control, White-Cell
Regulation
21 CFR 864.8625
Device class
Class II
Review panel
Hematology
Applicant
Elite Diagnostic , Ltd. 3244 Dogwood Cir. So. Dr., Indianapolis IN
Third party review
No

Clearances, product code GGL

Trailing 12 months

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

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