Angiomed U.S., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K874771ANGIOMED INTRODUCING SETSJanuary 12, 1988
K874585ANGIOMED OSTY-CUT BONE BIOPSY NEEDLEDecember 2, 1987
K864225ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENTJanuary 30, 1987
K863386VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETSOctober 24, 1986
K862805ANGIOMED VAC-U-CUT BIOPSY NEEDLESeptember 29, 1986
K863446ANGIOMED HIGH PRESSURE CONNECTORSSeptember 23, 1986
K854910ANGIOFLOWJuly 17, 1986
K854912ANGIOMED GUIED WIRESApril 16, 1986
K854908UROFLEXMarch 14, 1986
K855142ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHYMarch 11, 1986
K855143ANGIOMED EXCHANGE DRAINAGE CATHETER SETSMarch 11, 1986
K855076ANGIOMED URETER DIATION SETSMarch 11, 1986
K860534BILE ENDOPROSTHESIS SETMarch 10, 1986
K855140ANGIOMED RENAL DILATION SETFebruary 24, 1986
K855078ANGIO MED DISPOSABLE PRESSURE CONNECTORSFebruary 19, 1986
K854652ANGIOMED URETERAL STONE DISLODGERSFebruary 10, 1986
K854911PERCUTANEOUS NEPHROSTOMY SETS (SCHULLER)January 24, 1986
K854906PERCUTANEOUS NEPHROSTOMY SETS (OTTO)January 24, 1986
K854905PERCUTANEOUS NEPHROSTOMY SETS (LOOP TECHNIQUE)January 24, 1986
K854909PEDIATRIC PERCUTANEOUS NEPHROSTOMY SETSJanuary 24, 1986