510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K820037Substantially Equivalent

Sickle-Check

Diagnostic Technology, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K820037 is the FDA 510(k) clearance record for SICKLE-CHECK, a class II device, cleared for Diagnostic Technology, Inc. on under FDA product code JCM (Control, Hemoglobin, Abnormal). FDA records list 28 510(k) clearances for Diagnostic Technology, Inc., from to . As of , FDA records show no recalls naming K820037.

Clearance record

Decision date
Received
(28 days to decision)
Product code
JCM Control, Hemoglobin, Abnormal
Regulation
21 CFR 864.7415
Device class
Class II
Review panel
Hematology
Applicant
Diagnostic Technology, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code JCM

Trailing 12 months

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

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