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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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