Output, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Output, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1976 to 1980. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Output, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Output, Inc.
5 devices
Cleared
Feb 29, 1980
OUTPUT DIGITAL DISPLAY MODULE, MOD. 611
Cardiovascular
9d
Cleared
Oct 06, 1978
PRINTER, DIGITAL
Cardiovascular
95d
Cleared
May 31, 1978
OUTPUT DIGITAL DISPLAY MODULE, MODEL 401
Cardiovascular
86d
Cleared
Jun 14, 1977
NERVE STIMULATOR, MOLEL NO. FB-800
Neurology
14d
Cleared
Nov 19, 1976
PERIPHERAL NERVE STIMULATOR
Anesthesiology
70d