Hirata Sangyo Co. USA, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Hirata Sangyo Co. USA, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1982 to 1986.
Browse the FDA 510(k) cleared devices submitted by Hirata Sangyo Co. USA, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Nov 19, 1986
SR-MODEL 230 (MODIFICATION)
General Hospital
29d
Cleared
Jul 25, 1984
SR- MODEL 230
General Hospital
47d
Cleared
Nov 28, 1983
SURGICAL INSTRUMENT
General & Plastic Surgery
62d
Cleared
Nov 28, 1983
SURGICAL INSTRUMENT
General & Plastic Surgery
62d
Cleared
Oct 14, 1983
MULTIPLE MANUAL SURGICAL INSTRUMENTS
Orthopedic
73d
Cleared
Jul 19, 1983
GP-303
Cardiovascular
63d
Cleared
Oct 18, 1982
NON-STETHO 7, UM-15TP
Cardiovascular
103d
Cleared
Oct 08, 1982
SYRINGE PUMP
General Hospital
45d