Lowenkamp Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lowenkamp Intl., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Lowenkamp Intl., Inc. has 4 FDA 510(k) cleared medical devices. Based in Hazlehurst, US.
Historical record: 4 cleared submissions from 1990 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Lowenkamp Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lowenkamp Intl., Inc.
4 devices
Cleared
Jun 28, 1995
PATIENT EXAMINATION GLOVE
General Hospital
64d
Cleared
Jan 11, 1995
MALA LATEX EXAM GLOVES AND SCAN-SUB
General Hospital
26d
Cleared
Feb 25, 1991
FOXELL PLUS MULTIPLE (PERSONAL TOUCH TM)
General Hospital
25d
Cleared
Sep 14, 1990
SANOFLEX-STERILE LATEX SURGICAL GLOVES
General Hospital
42d