Porges Corp. is one of 15119 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Porges Corp. - FDA 510(k) Cleared Devices
Recent clearances: PORGES DORMIA 3 FR FLAT WIRE BASKET STONE DISLODGE, MODIFIED PEDIATRIC SILICONE FOLEY CATHETERS, PORGES ERCP CATHETERS
18
Total
18
Cleared
0
Denied
Porges Corp. has 18 FDA 510(k) cleared gastroenterology & urology devices. Based in Stamford, US.
Historical record: 18 cleared submissions from 1988 to 1990.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Porges Corp.
18 devices
Cleared
Jul 03, 1990
PORGES DORMIA 3 FR FLAT WIRE BASKET STONE DISLODGE
Gastroenterology & Urology
166d
Cleared
Mar 06, 1990
MODIFIED PEDIATRIC SILICONE FOLEY CATHETERS
Gastroenterology & Urology
61d
Cleared
Jan 30, 1990
PORGES ERCP CATHETERS
Gastroenterology & Urology
76d
Cleared
Jan 30, 1990
PORGES UNIVERSAL HANDLES
Gastroenterology & Urology
76d
Cleared
Jan 29, 1990
PORGES CYTOLOGY BRUSHES
Gastroenterology & Urology
82d
Cleared
Jan 29, 1990
PORGES DIATHERMY SNARE
Gastroenterology & Urology
75d
Cleared
Jan 26, 1990
PORGES SCLEROTHERAPY NEEDLES
Gastroenterology & Urology
79d
Cleared
Jan 26, 1990
PORGES 2-WAY BALLOON EXTRACTION CATHETER
Gastroenterology & Urology
72d
Cleared
Jan 26, 1990
PORGES ENDOSCOPIC DORMIA EXTRACTORS, DORMIATRIPTOR
Gastroenterology & Urology
72d
Cleared
Jan 22, 1990
PORGES NASOBILIARY DRAIN
Gastroenterology & Urology
77d
Cleared
Jan 22, 1990
PORGES BILIARY STENTS
Gastroenterology & Urology
75d
Cleared
Jan 22, 1990
PORGES SPHINCTEROTOMES
Gastroenterology & Urology
75d