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
K233115 09/27/2023 Hawkeye Control Unit with Eyas Endoscope E Surgical, LLC


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