Last synced on 14 November 2025 at 11:06 pm

Lyka® PORT Needle Free Access Device (4170Y)

Page Type
Cleared 510(K)
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)
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