510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993375Substantially Equivalent

Cds Ltx Control Latex Particle Suspension and Primer

Clinical Diagnostic Solutions, Inc., Plantation FL / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K993375 is the FDA 510(k) clearance record for CDS LTX CONTROL LATEX PARTICLE SUSPENSION AND PRIMER, a class II device, cleared for Clinical Diagnostic Solutions, Inc. on under FDA product code KRX (Calibrator For Cell Indices). FDA records list 3 510(k) clearances for Clinical Diagnostic Solutions, Inc., from to . As of , FDA records show no recalls naming K993375.

Clearance record

Decision date
Received
(74 days to decision)
Product code
KRX Calibrator For Cell Indices
Regulation
21 CFR 864.8150
Device class
Class II
Review panel
Hematology
Applicant
Clinical Diagnostic Solutions, Inc. 1660 NW 65th Ave. Suite 2, Plantation FL
510(k) summary
Summary
Third party review
No

Clearances, product code KRX

Trailing 12 months

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

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