STERiJECT Low Dead Space, STERiJECT The Invisible Needle— 510(k) K231734
Substantially EquivalentTsk Laboratory International Japan KK
FDA 510(k) clearance K231734 for STERiJECT Low Dead Space, STERiJECT The Invisible Needle, Substantially Equivalent on 2024-03-08. Applicant: Tsk Laboratory International Japan KK. Device class: 2.
Clearance details
- Applicant
- Tsk Laboratory International Japan KK
- Product code
- Code QNS
- Device class
- Class 2
- Regulation
- 21 CFR 880.5570
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tochigi-Shi, JP
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