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Worker Guidewire

Page Type
Cleared 510(K)
510(k) Number
K160785
510(k) Type
Traditional
Applicant
ARGON MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2016
Days to Decision
261 days
Submission Type
Summary

Worker Guidewire

Page Type
Cleared 510(K)
510(k) Number
K160785
510(k) Type
Traditional
Applicant
ARGON MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2016
Days to Decision
261 days
Submission Type
Summary