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FEELject LDV (Low dead volume) syringe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213010
510(k) Type
Traditional
Applicant
Feeltech Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/31/2023
Days to Decision
618 days
Submission Type
Summary

FEELject LDV (Low dead volume) syringe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213010
510(k) Type
Traditional
Applicant
Feeltech Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/31/2023
Days to Decision
618 days
Submission Type
Summary