Egnell, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Egnell, Inc. - FDA 510(k) Cleared Devices
10
Total
8
Cleared
0
Denied
Egnell, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1981 to 1985. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Egnell, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Egnell, Inc.
10 devices
Cleared
Nov 25, 1985
EGNELL UNIVERSAL SUCTION PUMP
General & Plastic Surgery
66d
Cleared
Nov 25, 1985
EGNELL COMPACT SUCTION PUMP
General & Plastic Surgery
63d
Cleared
Feb 04, 1985
EGNELL-LACT B BATTERY-OPERATED BREAST PUMP
Obstetrics & Gynecology
98d
Cleared
Apr 30, 1984
AMETHERM
General Hospital
83d
Cleared
Apr 20, 1984
AMEDA PHOTOTHERAPY LAMP FOR NEWBORN
General Hospital
130d
Cleared
Dec 22, 1983
AMEDA NEONATAL RESUSCITATION UNIT-
General Hospital
140d
Cleared
Dec 31, 1981
UNIVERSAL SUCTION PUMP TYPE EUS
General & Plastic Surgery
37d
Cleared
Dec 09, 1981
GASTRIC JUICES SUCTION PUMP
General & Plastic Surgery
36d
Cleared
Dec 02, 1981
PE-01 ELECTRONIC INFUSION PUMP
General Hospital
47d
Cleared
Oct 20, 1981
EGNELL COMPACT, TYPE EHV
General & Plastic Surgery
92d