E Surgical, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Known Names

e surgical, e. surgical

Recent 510(k) Clearances

K-NumberDeviceDate
K233115Hawkeye Control Unit with Eyas EndoscopeFebruary 6, 2024
K231126Eblator DeviceAugust 2, 2023
K071080ELECTROSURGICAL INFANT PATIENT RETURN ELECTRODE, DUAL PLATE WITH CORD, MODEL EP 211MAugust 31, 2007
K061878ELECTRODE COATED BALL, MODEL AB302C; NEEDLE, MODEL AN301C; BLADE, MODEL AE301HCOctober 24, 2006
K060255E SURGICAL ELECTROSURGICAL PATIENT RETURN ELECTRODE, DUAL PLATE WITH CORD AND ELECTROSURGICAL PATIENMarch 31, 2006