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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name instrument, manual, general obstetric-gynecologic
510(k) Number K823792
Device Name QUARTZ RETRACTOR/PROBE
Applicant
AMERICAN V. MUELLER
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
AMERICAN V. MUELLER
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number884.4520
Classification Product Code
KOH  
Date Received12/15/1982
Decision Date 01/18/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
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