A5 Anesthesia System (A5); A7 Anesthesia System (A7)
K-Number: K253330 · 2026-06-25
Device Summary
Frequently Asked Questions
What is the A5 Anesthesia System (A5); A7 Anesthesia System (A7)?
A5 Anesthesia System (A5); A7 Anesthesia System (A7) is a medical device that received FDA 510(k) clearance on 2026-06-25. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K253330.
When did A5 Anesthesia System (A5); A7 Anesthesia System (A7) receive FDA 510(k) clearance?
A5 Anesthesia System (A5); A7 Anesthesia System (A7) received FDA 510(k) clearance on 2026-06-25, under 510(k) number K253330.
Who is the listed applicant for A5 Anesthesia System (A5); A7 Anesthesia System (A7)?
The FDA 510(k) record lists Shenzhen Mindray Bio-Medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A5 Anesthesia System (A5); A7 Anesthesia System (A7)?
The FDA product code for A5 Anesthesia System (A5); A7 Anesthesia System (A7) is BSZ.
Other records listing Shenzhen Mindray Bio-Medical Electronics Co., Ltd. as applicant
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.
Related Devices (Code: BSZ)
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.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.