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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name conformer, ophthalmic
510(k) Number K921229
Device Name STERILE/SINGLE USE OPHTHALMIC CONFORMERS
Applicant
STORZ INSTRUMENT CO.
3365 TREE CT. INDUSTRIAL BLVD.
ST. LOUIS,  MO  63122 -6694
Applicant Contact JANET LACAVICH
Correspondent
STORZ INSTRUMENT CO.
3365 TREE CT. INDUSTRIAL BLVD.
ST. LOUIS,  MO  63122 -6694
Correspondent Contact JANET LACAVICH
Regulation Number886.3130
Classification Product Code
HQN  
Date Received03/13/1992
Decision Date 06/09/1992
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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