FDA 510(k) Applications Submitted by BERNARD ACKERMAN

FDA 510(k) Number Submission Date Device Name Applicant
K940176 01/11/1994 ACKRAD IUI SET FOR INTRAUTERINE INSEMINATION ACKRAD LABORATORIES
K961752 05/06/1996 H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607) ACKRAD LABORATORIES
K970492 02/10/1997 INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER ACKRAD LABORATORIES


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