Sears, Roebuck & Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sears, Roebuck & Co. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Sears, Roebuck & Co. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1977 to 1981. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sears, Roebuck & Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sears, Roebuck & Co.
6 devices
Cleared
May 08, 1981
ELECTRODE BLOOD PRESSURE MONITOR
Cardiovascular
59d
Cleared
Apr 29, 1980
DIGITAL ELECTRONIC B.P. MONITOR 2155
Cardiovascular
21d
Cleared
Jan 28, 1980
DIGITAL ELECTRONIC EXERCISER/PULSE MTR.
Physical Medicine
14d
Cleared
Dec 04, 1978
BLOOD PRESSURE, DIGITAL MODEL #2153
Cardiovascular
55d
Cleared
Jul 18, 1978
DIGITAL BLOOD PRESSURE MONITOR
Cardiovascular
34d
Cleared
Sep 30, 1977
SPHYGMOMANOMETER #1235
Cardiovascular
30d