510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955719Substantially Equivalent

Sickle-2000

Medicus Technologies, Inc., West Chester PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955719 is the FDA 510(k) clearance record for SICKLE-2000, a class II device, cleared for Medicus Technologies, Inc. on under FDA product code GIQ (Hemoglobin S). FDA records list one 510(k) clearance for Medicus Technologies, Inc. As of , FDA records show no recalls naming K955719.

Clearance record

Decision date
Received
(240 days to decision)
Product code
GIQ Hemoglobin S
Regulation
21 CFR 864.7415
Device class
Class II
Review panel
Hematology
Applicant
Medicus Technologies, Inc. 515 S. Franklin St., West Chester PA
510(k) summary
Summary
Third party review
No

Clearances, product code GIQ

Trailing 12 months

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

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