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FDA 510(k)

Cryojet Plus (SHE-ACP001-1)

K-Number: K233416 · 2024-02-06

Decision Date2024-02-06
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Cryojet Plus (SHE-ACP001-1) is a medical device manufactured by Beijing Sano Laser S&T Development Co.,Ltd. It received FDA 510(k) clearance on 2024-02-06 under approval number K233416. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cryojet Plus (SHE-ACP001-1)?

Cryojet Plus (SHE-ACP001-1) is a medical device that received FDA 510(k) clearance on 2024-02-06. It is manufactured by Beijing Sano Laser S&T Development Co.,Ltd. The 510(k) number is K233416.

When was Cryojet Plus (SHE-ACP001-1) approved by the FDA?

Cryojet Plus (SHE-ACP001-1) received FDA 510(k) clearance on 2024-02-06, under approval number K233416.

What company makes Cryojet Plus (SHE-ACP001-1)?

Cryojet Plus (SHE-ACP001-1) is manufactured by Beijing Sano Laser S&T Development Co.,Ltd.

What is the FDA product code for Cryojet Plus (SHE-ACP001-1)?

The FDA product code for Cryojet Plus (SHE-ACP001-1) is GEX. This falls under the Gastroenterology category.

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Official Source

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