Aspen Labs

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K970493HYFRECATOR 2000April 30, 1997
K925333SINGLE USE TUNGSTEN WIRE LEE LOOP ELECTRODESeptember 27, 1994
K931215HAND-TROL SMarch 28, 1994
K912046SINGLE USE LEE ELECTRODEMarch 5, 1992
K905654ELECTROSURGICAL UNIT WITH ACCESSORIESMarch 18, 1991
K904240SINGLE USE LAPARSCOPIC ELECTRODEFebruary 19, 1991