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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K854872
Device Name VFI/VFE SYSTEM II
Applicant
Mira, Inc.
87 Rumford Ave.
Waltham,  MA  02453 -3846
Applicant Contact MARK W FURLONG
Correspondent
Mira, Inc.
87 Rumford Ave.
Waltham,  MA  02453 -3846
Correspondent Contact MARK W FURLONG
Date Received12/04/1985
Decision Date 02/13/1986
Decision Substantially Equivalent (SESE)
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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