Greenleaf Medical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Greenleaf Medical Systems, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Greenleaf Medical Systems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 4 cleared submissions from 1989 to 1995. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Greenleaf Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Greenleaf Medical Systems, Inc.
4 devices
Cleared
May 15, 1995
DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)
Neurology
276d
Cleared
Apr 15, 1994
GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEM
Neurology
140d
Cleared
Oct 10, 1989
GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM
Neurology
155d
Cleared
Feb 08, 1989
(DATAGLOVE) HAND IMPAIRMENT EVALUATION SYSTEM
Neurology
90d