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subpart-f—therapeutic-devices/

PROCLEAR COMPATIBLES MULTIFOCAL

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K032873
510(k) Type: Traditional
Applicant: COOPER VISION, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 11/7/2003
Days to Decision: 53 days
Submission Type: Summary

FDA Browser

subpart-f—therapeutic-devices/

PROCLEAR COMPATIBLES MULTIFOCAL

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K032873
510(k) Type: Traditional
Applicant: COOPER VISION, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 11/7/2003
Days to Decision: 53 days
Submission Type: Summary