510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K232493Substantially Equivalent

Embryo Real-time Incubator (TLS301), Embryo Real-time Culture Dish (MC 2004)

Wuhan Huchuang Union Technology Co., Ltd., Wuhan, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K232493 is the FDA 510(k) clearance record for Embryo Real-time Incubator (TLS301), Embryo Real-time Culture Dish (MC 2004), a class II device, cleared for Wuhan Huchuang Union Technology Co., Ltd. on under FDA product code MQG (Accessory, Assisted Reproduction). FDA records list one 510(k) clearance for Wuhan Huchuang Union Technology Co., Ltd. As of , FDA records show no recalls naming K232493.

Clearance record

Decision date
Received
(264 days to decision)
Product code
MQG Accessory, Assisted Reproduction
Regulation
21 CFR 884.6120
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Wuhan Huchuang Union Technology Co., Ltd. Bldg. 10, #818 Gaoxin Ave., Wuhan, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MQG

Trailing 12 months
2 clearances under product code MQG in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MQG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260