510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K223690Substantially Equivalent

iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C)

Shenzhen Yhlo Biotech Co., Ltd., Shenzhen, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K223690 is the FDA 510(k) clearance record for iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C), a class II device, cleared for Shenzhen Yhlo Biotech Co., Ltd. on under FDA product code DHA (System, Test, Human Chorionic Gonadotropin). FDA records list one 510(k) clearance for Shenzhen Yhlo Biotech Co., Ltd. As of , FDA records show no recalls naming K223690.

Clearance record

Decision date
Received
(367 days to decision)
Product code
DHA System, Test, Human Chorionic Gonadotropin
Regulation
21 CFR 862.1155
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Shenzhen Yhlo Biotech Co., Ltd. Bldg. 1, Yhlo Biopark, Baolong 2nd Rd., Shenzhen, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DHA

Trailing 12 months

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

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