FEELject LDV (Low dead volume) syringe— 510(k) K213010

Substantially Equivalent

Feeltech Co., Ltd.

FDA 510(k) clearance K213010 for FEELject LDV (Low dead volume) syringe, Substantially Equivalent on 2023-05-31. Applicant: Feeltech Co., Ltd..

Clearance details

Applicant: Feeltech Co., Ltd.
Product code: Code QNQ
Advisory panel: General Hospital
Date received: 2021-09-20
Decision date: 2023-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gunsan-Si, KR

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