STERiJECT Low Dead Space, STERiJECT The Invisible Needle
K-Number: K231734 · 2024-03-08
Device Summary
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. The listed applicant is Tsk Laboratory International Japan KK. The 510(k) number is K231734.
When did STERiJECT Low Dead Space, STERiJECT The Invisible Needle receive FDA 510(k) clearance?
STERiJECT Low Dead Space, STERiJECT The Invisible Needle received FDA 510(k) clearance on 2024-03-08, under 510(k) number K231734.
Who is the listed applicant for STERiJECT Low Dead Space, STERiJECT The Invisible Needle?
The FDA 510(k) record lists Tsk Laboratory International Japan KK as the applicant. This does not by itself establish the device manufacturer.
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 records listing Tsk Laboratory International Japan KK 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: QNS)
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.