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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Fertility Diagnostic, Proceptive
510(k) Number K823463
Device Name RIGHT TIME RHYTHM CLOCK
Applicant
P.K. MORGAN INSTRUMENTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
P.K. MORGAN INSTRUMENTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Classification Product Code
LHD  
Date Received11/19/1982
Decision Date 03/17/1983
Decision Substantially Equivalent (SESE)
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
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