Kinsei Shiatsu, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kinsei Shiatsu, Inc. - FDA 510(k) Cleared Devices
6
Total
1
Cleared
0
Denied
Kinsei Shiatsu, Inc. has 1 FDA 510(k) cleared medical devices. Based in Torrance, US.
Historical record: 1 cleared submissions from 1995 to 1995. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Kinsei Shiatsu, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kinsei Shiatsu, Inc.
6 devices
Cleared
Sep 29, 1995
SPIN ROLLERE
Physical Medicine
93d
Cleared
Aug 28, 1995
SHIATSU MASTER MASSAGER CUSHION
Physical Medicine
63d
Cleared
Aug 02, 1995
RELAXU-1
Physical Medicine
183d
Cleared
Feb 14, 1995
RELAXY-WONDER KNOCK
Physical Medicine
19d
Cleared
Feb 14, 1995
SHAPE UP MOMI ROLLER
Physical Medicine
19d
Cleared
Feb 14, 1995
RELAXY-THE WONDER HAND
Physical Medicine
19d