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Lyka® PORT Needle Free Access Device (4170Y)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241058
510(k) Type
Traditional
Applicant
Quest Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2024
Days to Decision
244 days
Submission Type
Summary

Lyka® PORT Needle Free Access Device (4170Y)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241058
510(k) Type
Traditional
Applicant
Quest Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2024
Days to Decision
244 days
Submission Type
Summary