Apothecary Products, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Apothecary Products, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Apothecary Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Burnsville, US.
Historical record: 6 cleared submissions from 1984 to 2014.
Browse the FDA 510(k) cleared devices submitted by Apothecary Products, Inc. Filter by specialty or product code using the sidebar.
Apothecary Products, Inc. — FDA 510(k) Products and Clearance History
6 devices
Cleared
Jul 09, 2014
FLENTS PLASTIC EYE WASH CUP
Ophthalmic
141d
Cleared
Jul 14, 2011
SOFT GRIP CONTACT LENS CASE, DELUXE CONTACT LENS CASE, ECONO-MATE CONTACT...
Ophthalmic
15d
Cleared
Nov 26, 2004
EZY-TRAVEL WRISTBAND
Neurology
149d
Cleared
Jun 25, 2002
ADULT SILICONE EAR PLUGS, MODELS # 68053, 68057
Ear, Nose, Throat
148d
Cleared
May 12, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
37d
Cleared
Feb 04, 1984
NITROGLYCERINE CONTAINER
General Hospital
131d