Last synced on 30 September 2022 at 11:05 pm

SOLUTIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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