FEELject LDV (Low dead volume) syringe— 510(k) K213010
Substantially EquivalentFeeltech Co., Ltd.
FDA 510(k) clearance K213010 for FEELject LDV (Low dead volume) syringe, Substantially Equivalent on 2023-05-31. Applicant: Feeltech Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Feeltech Co., Ltd.
- Product code
- Code QNQ
- Device class
- Class 2
- Regulation
- 21 CFR 880.5860
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Gunsan-Si, KR
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More clearances from Feeltech Co., Ltd.
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