Hirata Sangyo Co. USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Hirata Sangyo Co. USA, Inc.
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