Cryojet Plus (SHE-ACP001-1)
K-Number: K233416 · 2024-02-06
Device Summary
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.
Other Devices by Beijing Sano Laser S&T Development Co.,Ltd
Related Devices (Code: GEX)
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.