Last synced on 14 November 2025 at 11:06 pm

SOLUTIS

Page Type
Cleared 510(K)
510(k) Number
K130933
510(k) Type
Traditional
Applicant
QUANTEL MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2013
Days to Decision
120 days
Submission Type
Summary

SOLUTIS

Page Type
Cleared 510(K)
510(k) Number
K130933
510(k) Type
Traditional
Applicant
QUANTEL MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2013
Days to Decision
120 days
Submission Type
Summary