Jomed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K031346JOVUS EAGLE EYE F/X 2.9F IVUS CATHETER, MODEL 85900June 23, 2003
K031148IN-VISION IMAGING SYSTEMMay 28, 2003
K031277JOWIRE ASAHI PTCA CATHETER GUIDE WIRES, MODELS AG145300,141300,142300,132200,14M350,14M345,14M360,14May 14, 2003
K030053JOSTENT SELFX, MODELS 015SX4406; 015SX4408; 015SX4410; 015SX680; 015SX6808; 015SX6810March 31, 2003
K022762JOWIRE NEO'S PTCA CATHETER GUIDEWIRES, MODELS AG141000, AG142000, AG143000, AG141002, AG141010, AG14December 16, 2002
K021219SMARTWIRE/SMARTMAP PRESSURE SYSTEMMay 17, 2002
K020854MODIFICATION TO FOX PTA CATHETERApril 11, 2002
K010838FOX PTA CATHETER, 3.0, 4.0, 5.0, 6.0, 7.0, AND 8.0 X 40 MM, MODELS A14003, A14004, A14005, A14006, AJune 21, 2001
K003938TRAK BACK IIJanuary 18, 2001