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Dual Action Tissue Closure Device

Page Type
Cleared 510(K)
510(k) Number
K250229
510(k) Type
Traditional
Applicant
Micro-Tech (Nanjing) Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/8/2025
Days to Decision
224 days
Submission Type
Summary

Dual Action Tissue Closure Device

Page Type
Cleared 510(K)
510(k) Number
K250229
510(k) Type
Traditional
Applicant
Micro-Tech (Nanjing) Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/8/2025
Days to Decision
224 days
Submission Type
Summary