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FDA 510(k)

Vacuum Pump (Model: AD-VPUM-500)

K-Number: K260194 · 2026-04-28

ApplicantSheng Sheng Yi (Beijing) Technology Company Limited
Decision Date2026-04-28
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Vacuum Pump (Model: AD-VPUM-500) is the device name listed in this FDA 510(k) record. The listed applicant is Sheng Sheng Yi (Beijing) Technology Company Limited. It received FDA 510(k) clearance on 2026-04-28 under 510(k) number K260194. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vacuum Pump (Model: AD-VPUM-500)?

Vacuum Pump (Model: AD-VPUM-500) is a medical device that received FDA 510(k) clearance on 2026-04-28. The listed applicant is Sheng Sheng Yi (Beijing) Technology Company Limited. The 510(k) number is K260194.

When did Vacuum Pump (Model: AD-VPUM-500) receive FDA 510(k) clearance?

Vacuum Pump (Model: AD-VPUM-500) received FDA 510(k) clearance on 2026-04-28, under 510(k) number K260194.

Who is the listed applicant for Vacuum Pump (Model: AD-VPUM-500)?

The FDA 510(k) record lists Sheng Sheng Yi (Beijing) Technology Company Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vacuum Pump (Model: AD-VPUM-500)?

The FDA product code for Vacuum Pump (Model: AD-VPUM-500) is MQG.

Related Devices (Code: MQG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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