Post Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Post Medical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Post Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1983 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Post Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Post Medical, Inc.
6 devices
Cleared
Apr 21, 1999
DIABETIC NEEDLE DISPOSAL, MODEL # PMSM - 950
General Hospital
72d
Cleared
Aug 15, 1997
SYRINGE NEEDLE REMOVER (S.N.R.)
General Hospital
68d
Cleared
May 09, 1994
AUTOMATIC NEEDLE DISCONECT (A.N.D.)
General Hospital
579d
Cleared
Apr 29, 1994
SHARPS CONTAINMENT SYSTEM
General Hospital
528d
Cleared
Apr 28, 1983
MALE EXTERNAL CATHETER
Gastroenterology & Urology
35d
Cleared
Apr 12, 1983
SYRINGE/NEEDLE DISPOS-BOX-CUTTER/CRIMPER
General & Plastic Surgery
19d