STERiJECT Low Dead Space, STERiJECT The Invisible Needle
K-Number: K231734 · 2024-03-08
Decision Date2024-03-08
Product CodeQNS
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
STERiJECT Low Dead Space, STERiJECT The Invisible Needle is a medical device manufactured by Tsk Laboratory International Japan KK. It received FDA 510(k) clearance on 2024-03-08 under approval number K231734. The device is classified under product code QNS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the STERiJECT Low Dead Space, STERiJECT The Invisible Needle?
STERiJECT Low Dead Space, STERiJECT The Invisible Needle is a medical device that received FDA 510(k) clearance on 2024-03-08. It is manufactured by Tsk Laboratory International Japan KK. The 510(k) number is K231734.
When was STERiJECT Low Dead Space, STERiJECT The Invisible Needle approved by the FDA?
STERiJECT Low Dead Space, STERiJECT The Invisible Needle received FDA 510(k) clearance on 2024-03-08, under approval number K231734.
What company makes STERiJECT Low Dead Space, STERiJECT The Invisible Needle?
STERiJECT Low Dead Space, STERiJECT The Invisible Needle is manufactured by Tsk Laboratory International Japan KK.
What is the FDA product code for STERiJECT Low Dead Space, STERiJECT The Invisible Needle?
The FDA product code for STERiJECT Low Dead Space, STERiJECT The Invisible Needle is QNS.
Other Devices by Tsk Laboratory International Japan KK
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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.