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subpart-f—therapeutic-devices/

CONTROLLED PROCESS RELEASE OF FLEXLENS (HEFILCON A)

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K970312
510(k) Type: Traditional
Applicant: FLEXLENS, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 4/2/1997
Days to Decision: 65 days
Submission Type: Statement

FDA Browser

subpart-f—therapeutic-devices/

CONTROLLED PROCESS RELEASE OF FLEXLENS (HEFILCON A)

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K970312
510(k) Type: Traditional
Applicant: FLEXLENS, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 4/2/1997
Days to Decision: 65 days
Submission Type: Statement