American Endoscopy, Inc.
American Endoscopy, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1985.
Top product codes for American Endoscopy, Inc.
- FGE — Gastroenterology, Urology
- KNS — Gastroenterology, Urology
- KOD — Gastroenterology, Urology
- FCL — Gastroenterology, Urology
- FFT — Gastroenterology, Urology
- GAA — General, Plastic Surgery
- GCP — Gastroenterology, Urology
- GEE — General, Plastic Surgery
- GEI — General, Plastic Surgery
- KNQ — Gastroenterology, Urology
Recent clearances by American Endoscopy, Inc.
- K853274 — AMERICAN DILATATION SYSTEM
- K841384 — PROXIMA 1 PH MONITOR
- K833491 — ENDO BITE BLOCK
- K840818 — BIOPSY FORCEPS
- K833859 — TAMPONADE BALLOON CUFF
- K833492 — PERCUTANEOUS ENDOSCOPIC GASTROSCOPY
- K832458 — AUTOMATIC ENDOSCOPE
- K821818 — RETRIEVAL BALLOONS
- K821819 — PIGTAIL STENTS
- K822062 — BALL TIP COAGULATING ELECTRODES
- K821817 — PIGTAIL NASAL CATHETERS
- K822061 — LAVAGING CATHETERS
- K821697 — INJECTION ASPIRATING NEEDLES
- K820431 — E.R.C.P. CANNULAS
- K820429 — SPIRAL STONE AND RETRIEVAL BASKETS
- K820430 — DIATHERMIC SNARES
- K820239 — RETRIEVAL FORCEPS
- K820240 — PAPILLOTOMES
- K820259 — STERILE CYTOLOGY BRUSHES
Data sourced from openFDA. This site is unofficial and independent of the FDA.