510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K260194Substantially Equivalent

Vacuum Pump (Model: AD-VPUM-500)

Sheng Sheng Yi (Beijing) Technology Company Limited, Beijing, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K260194 is the FDA 510(k) clearance record for Vacuum Pump (Model: AD-VPUM-500), a class II device, cleared for Sheng Sheng Yi (Beijing) Technology Company Limited on under FDA product code MQG (Accessory, Assisted Reproduction). FDA records list one 510(k) clearance for Sheng Sheng Yi (Beijing) Technology Company Limited. As of , FDA records show no recalls naming K260194.

Clearance record

Decision date
Received
(96 days to decision)
Product code
MQG Accessory, Assisted Reproduction
Regulation
21 CFR 884.6120
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Sheng Sheng Yi (Beijing) Technology Company Limited Rm.235-238, Jianjin Ctr, # Jia 1, Yongtaiyuan, Qinghe, Beijing, 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