Sinochem (Usa), Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sinochem (Usa), Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Sinochem (Usa), Inc. has 14 FDA 510(k) cleared general hospital devices. Based in New York, US.
Historical record: 14 cleared submissions from 1989 to 1990.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sinochem (Usa), Inc.
14 devices
Cleared
Jun 01, 1990
LATEX EXAMINATION GLOVES
General Hospital
91d
Cleared
May 16, 1990
LATEX SURGEON GLOVES
General Hospital
51d
Cleared
Mar 27, 1990
LATEX EXAM GLOVES (SHANGHAI RONGTONG LATEX GLOVES)
General Hospital
63d
Cleared
Sep 21, 1989
LATEX EXAMINATION GLOVES
General Hospital
118d
Cleared
Aug 10, 1989
LATEX EXAM GLOVES(MFG: SHANG HAI RONGTONG LATEX)
General Hospital
86d
Cleared
Jul 14, 1989
PATIENT EXAM GLOVES (MFG. GUILIN LATEX FACTORY)
General Hospital
100d
Cleared
Jul 14, 1989
PATIENT EXAM GLOVES (MFG. JIANDE RUBBER PRODUCTS)
General Hospital
100d
Cleared
Jul 14, 1989
PATIENT EXAM GLOVES (MFG. LIAONING FOREIGN TRADE)
General Hospital
100d
Cleared
Jul 14, 1989
PATIENT EXAM GLOVES (MFG. HUBEI TIANMEN LATEX)
General Hospital
100d
Cleared
Jul 14, 1989
PATIENT EXAM GLOVES (MFG. NO. 1 FACTORY, WUHAN)
General Hospital
100d
Cleared
Jul 14, 1989
PATIENT EXAM GLOVES (MFG. RONGCHENG LATEX PRODUCT)
General Hospital
100d
Cleared
Jul 14, 1989
PATIENT EXAM GLOVES (MFG. SUZHOU LATEX FACTORY)
General Hospital
100d