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ProKnow DS

Page Type
Cleared 510(K)
510(k) Number
K182855
510(k) Type
Traditional
Applicant
ProKnow LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2019
Days to Decision
84 days
Submission Type
Summary

ProKnow DS

Page Type
Cleared 510(K)
510(k) Number
K182855
510(k) Type
Traditional
Applicant
ProKnow LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2019
Days to Decision
84 days
Submission Type
Summary