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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Source, Carrier, Fiberoptic Light
510(k) Number K930123
Device Name ASPIRATING ENDO OCULAR PROBE
Applicant
SURGICAL TECHNOLOGIES, INC.
750 GODDARD AVE.
CHESTERFIELD,  MO  63005
Applicant Contact ALAN T BECKMAN
Correspondent
SURGICAL TECHNOLOGIES, INC.
750 GODDARD AVE.
CHESTERFIELD,  MO  63005
Correspondent Contact ALAN T BECKMAN
Regulation Number874.4350
Classification Product Code
EQH  
Date Received01/12/1993
Decision Date 02/16/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
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