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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Instrument, Vitreous Aspiration And Cutting, Ac-Powered
510(k) Number K932669
Device Name SUPRA-VIT(TM)
Applicant
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC.
2235 POLVOROSA AVE.
SUITE 200
SAN LEANDRO,  CA  94577
Applicant Contact ERIK W PETERSON
Correspondent
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC.
2235 POLVOROSA AVE.
SUITE 200
SAN LEANDRO,  CA  94577
Correspondent Contact ERIK W PETERSON
Regulation Number886.4150
Classification Product Code
HQE  
Date Received06/02/1993
Decision Date 06/03/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
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