Angiomed U.S., Inc.
Angiomed U.S., Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1988.
Top product codes for Angiomed U.S., Inc.
Recent clearances by Angiomed U.S., Inc.
- K874771 — ANGIOMED INTRODUCING SETS
- K874585 — ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE
- K864225 — ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT
- K863386 — VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETS
- K862805 — ANGIOMED VAC-U-CUT BIOPSY NEEDLE
- K863446 — ANGIOMED HIGH PRESSURE CONNECTORS
- K854910 — ANGIOFLOW
- K854912 — ANGIOMED GUIED WIRES
- K854908 — UROFLEX
- K855076 — ANGIOMED URETER DIATION SETS
- K855142 — ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY
- K855143 — ANGIOMED EXCHANGE DRAINAGE CATHETER SETS
- K860534 — BILE ENDOPROSTHESIS SET
- K855140 — ANGIOMED RENAL DILATION SET
- K855078 — ANGIO MED DISPOSABLE PRESSURE CONNECTORS
- K854652 — ANGIOMED URETERAL STONE DISLODGERS
- K854905 — PERCUTANEOUS NEPHROSTOMY SETS (LOOP TECHNIQUE)
- K854906 — PERCUTANEOUS NEPHROSTOMY SETS (OTTO)
- K854907 — PERCUTANEOUS NEPHROSTOMY SETS (GUNTHER)
- K854909 — PEDIATRIC PERCUTANEOUS NEPHROSTOMY SETS
- K854911 — PERCUTANEOUS NEPHROSTOMY SETS (SCHULLER)
- K855104 — ANGIOMED SKIN FASCIA KNIFE
- K855141 — ANGIOMED FINE NEEDLES AND NEEDLE SET
- K855077 — ANGIOMED HARZMANN DISCS
Data sourced from openFDA. This site is unofficial and independent of the FDA.