Porges Corp.
Porges Corp. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1990.
Top product codes for Porges Corp.
- FGE — Gastroenterology, Urology
- KNS — Gastroenterology, Urology
- FBK — Gastroenterology, Urology
- FDX — Gastroenterology, Urology
- FFL — Gastroenterology, Urology
- GCP — Gastroenterology, Urology
- KGE — Gastroenterology, Urology
- KNQ — Gastroenterology, Urology
- KNY — Gastroenterology, Urology
- KOB — Gastroenterology, Urology
Recent clearances by Porges Corp.
- K900269 — PORGES DORMIA 3 FR FLAT WIRE BASKET STONE DISLODGE
- K900031 — MODIFIED PEDIATRIC SILICONE FOLEY CATHETERS
- K896503 — PORGES ERCP CATHETERS
- K896505 — PORGES UNIVERSAL HANDLES
- K896425 — PORGES CYTOLOGY BRUSHES
- K896507 — PORGES DIATHERMY SNARE
- K896424 — PORGES SCLEROTHERAPY NEEDLES
- K896504 — PORGES 2-WAY BALLOON EXTRACTION CATHETER
- K896506 — PORGES ENDOSCOPIC DORMIA EXTRACTORS, DORMIATRIPTOR
- K896376 — PORGES NASOBILIARY DRAIN
- K896423 — PORGES BILIARY STENTS
- K896426 — PORGES SPHINCTEROTOMES
- K896502 — PORGES BIOPSY & FOREIGN BODY FORCEPS
- K896537 — PORGES HOT BIOPSY FORCEPS
- K892383 — BILIARY ENDOPROSTHESIS FOR INTERNAL DRAINAGE SET
- K892384 — BILIARY ENDOPROSTHESIS AND EXTERNAL CATHETER
- K883526 — PORGES STEPPED NEOPLEX DILATOR
- K881097 — SPEC 5* SUPRAPUBIC CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.