Class Class II

Dual Action Tissue Closure Device (K250229)

K250229 2025-09-08 Traditional
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Description

Dual Action Tissue Closure Device by Micro-Tech (Nanjing) Co., Ltd., an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250229
Clearance Date2025-09-08
Clearance TypeTraditional
Product CodePKL
Regulation Number876.4400

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