Endotherapeutics

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Known Names

endo-therapeutics, endotherapeutics

Recent 510(k) Clearances

K-NumberDeviceDate
K870855UROSCANJune 9, 1987
K860192ENDOPORT 5MM SINGLE-USE TROCAR AND SLEEVEMarch 17, 1986
K860103MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVEFebruary 12, 1986
K860102MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLEFebruary 12, 1986
K852031ENDOPORT 5MMAugust 13, 1985
K844619ENDONEEDLEJanuary 9, 1985
K841716ENDOPORT EROCARJune 28, 1984