MODELS A21-A & A21-B POSTERIOR CHAMBER INTRAOCULAR

FDA Premarket Approval P900053

Pre-market Approval Supplement Details

• Device: MODELS A21-A & A21-B POSTERIOR CHAMBER INTRAOCULAR
• Generic Name: Intraocular Lens
• Applicant: VISION TECHNOLOGIES INTL., INC.
• Date Received: 1990-08-07
• Decision Date: 1991-02-28
• Notice Date: 1991-02-28
• PMA: P900053
• Supplement: S
• Product Code: HQL
• Docket Number: 91M-0089
• Advisory Committee: Ophthalmic
• Expedited Review: No
• Combination Product: No
• Applicant Address: VISION TECHNOLOGIES INTL., INC. 102 South Tejon suite 1100 colorado Springs, CO 80903

Supplemental Filings

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Supplement Number	Date	Supplement Type
P900053		Original Filing