Angiomed U.S., Inc. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
FDA 510(k) Regulatory Record - Angiomed U.S., Inc. General & Plastic Surgery ✕
12 devices
Cleared
Dec 02, 1987
ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE
General & Plastic Surgery
23d
Cleared
Sep 29, 1986
ANGIOMED VAC-U-CUT BIOPSY NEEDLE
General & Plastic Surgery
69d
Cleared
Sep 23, 1986
ANGIOMED HIGH PRESSURE CONNECTORS
General & Plastic Surgery
15d
Cleared
Mar 10, 1986
BILE ENDOPROSTHESIS SET
General & Plastic Surgery
26d
Cleared
Feb 19, 1986
ANGIO MED DISPOSABLE PRESSURE CONNECTORS
General & Plastic Surgery
62d
Cleared
Jan 24, 1986
PERCUTANEOUS NEPHROSTOMY SETS (LOOP TECHNIQUE)
General & Plastic Surgery
46d
Cleared
Jan 24, 1986
PERCUTANEOUS NEPHROSTOMY SETS (OTTO)
General & Plastic Surgery
Cleared
Jan 24, 1986
PERCUTANEOUS NEPHROSTOMY SETS (GUNTHER)
General & Plastic Surgery
46d
Cleared
Jan 24, 1986
PEDIATRIC PERCUTANEOUS NEPHROSTOMY SETS
General & Plastic Surgery
46d
Cleared
Jan 24, 1986
PERCUTANEOUS NEPHROSTOMY SETS (SCHULLER)
General & Plastic Surgery
46d
Cleared
Jan 24, 1986
ANGIOMED SKIN FASCIA KNIFE
General & Plastic Surgery
32d
Cleared
Jan 24, 1986
ANGIOMED FINE NEEDLES AND NEEDLE SET
General & Plastic Surgery
29d