Shargh Pharmaceutical Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shargh Pharmaceutical Co., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Shargh Pharmaceutical Co., Inc. has 5 FDA 510(k) cleared medical devices. Based in Culver City, US.
Historical record: 5 cleared submissions from 1990 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Shargh Pharmaceutical Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Shargh Pharmaceutical Co., Inc.
5 devices
Cleared
Jan 07, 2002
SHARGHP A.V. FISTULA NEEDLE SET
Gastroenterology & Urology
87d
Cleared
Sep 07, 1990
SHARGHP SYRINGES, WITH AND WITHOUT NEEDLE
General Hospital
343d
Cleared
Sep 07, 1990
SHARGHP HYPODERMIC NEEDLE
General Hospital
343d
Cleared
Sep 07, 1990
SHARGHP INTRAVENOUS CATHETER
General Hospital
343d
Cleared
Sep 07, 1990
SHARGHP INSULIN SYRINGES
General Hospital
343d