Panasonic Co. Div. Matsu Elec. Corp. America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Panasonic Co. Div. Matsu Elec. Corp. America - FDA 510(k) Cleared Dev...
9
Total
9
Cleared
0
Denied
Panasonic Co. Div. Matsu Elec. Corp. America has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1982 to 1986. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Panasonic Co. Div. Matsu Elec. Corp. America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Panasonic Co. Div. Matsu Elec. Corp. America
9 devices
Cleared
Jul 01, 1986
PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP
Cardiovascular
131d
Cleared
Oct 26, 1984
ELECTRONIC BLOOD PRESS. METER EN-212
Cardiovascular
486d
Cleared
Oct 26, 1984
NONINVASIVE BLOOD PRESSURE MEASURE SYS
Cardiovascular
226d
Cleared
Nov 14, 1983
PANASONIC WH-50 HEARING AID
Ear, Nose, Throat
34d
Cleared
Aug 12, 1983
ELECTRONIC BLOOD PRESS. METER-ZH-820P
Cardiovascular
45d
Cleared
Aug 11, 1983
PANASONIC MODEL EW-213
Cardiovascular
125d
Cleared
Apr 28, 1983
PANASONIC MODEL HV-5
General Hospital
20d
Cleared
Nov 29, 1982
MODEL WHO1 HEARING AID
Ear, Nose, Throat
25d
Cleared
Jul 20, 1982
HEARING AID VARIOUS MODELS
Ear, Nose, Throat
18d