FDA 510(k) Applications Submitted by E Surgical, LLC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K071080 |
04/17/2007 |
ELECTROSURGICAL INFANT PATIENT RETURN ELECTRODE, DUAL PLATE WITH CORD, MODEL EP 211M |
E SURGICAL, LLC |
K060255 |
02/01/2006 |
E SURGICAL ELECTROSURGICAL PATIENT RETURN ELECTRODE, DUAL PLATE WITH CORD AND ELECTROSURGICAL PATIENT RETURN ELECTRODE |
E SURGICAL, LLC |
K061878 |
07/03/2006 |
ELECTRODE COATED BALL, MODEL AB302C; NEEDLE, MODEL AN301C; BLADE, MODEL AE301HC |
E SURGICAL, LLC |
K231126 |
04/20/2023 |
Eblator Device |
E Surgical, LLC |
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