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subpart-f—therapeutic-devices/

PROCLEAR, PROCLEAR TORIC, PROCLEAR MULTIFOCAL, PROCLEAR 1DAY, PROCLEAR XC

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K111966
510(k) Type: Special
Applicant: COOPERVISION, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 9/15/2011
Days to Decision: 66 days
Submission Type: Summary

FDA Browser

subpart-f—therapeutic-devices/

PROCLEAR, PROCLEAR TORIC, PROCLEAR MULTIFOCAL, PROCLEAR 1DAY, PROCLEAR XC

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K111966
510(k) Type: Special
Applicant: COOPERVISION, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 9/15/2011
Days to Decision: 66 days
Submission Type: Summary