510(k) K970961

Device
VAPORIZATION ELECTRODES
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
510(k) number
K970961
Product code
KNF  
Decision
Substantially Equivalent (SESE)
Decision date
1998-04-10
Date received
1997-03-17
Regulation
884.4160
Classification name
Coagulator-cutter, Endoscopic, Unipolar (and Accessories)
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
ROBERT L CASARSA
Address
353 Corporate Woods Pkwy. Vernon Hills IL US 60061 60061

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code KNF  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K250705Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.2025-04-02
K240503Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.2024-07-17
K233848Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)Gynesonics, Inc.2023-12-21
K222304Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.2022-11-08
K211535Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.2021-06-17
K193516Sonata® Sonography-Guided Transcervical Fibroid Ablation System 2.1Gynesonics, Inc.2020-05-04
K173703Sonata Sonography-Guided Transcervical Fibroid Ablation SystemGynesonics, Inc.2018-08-15
K132135LINA GOLD LOOP HCLina Medical Aps2014-01-31
K121343MODULAP LOOPAtc Technologies, Inc.2013-06-14
K103726JARIT TAKE-APART ENDOSCOPIC INSTRUMENTSIntegra LifeSciences Corporation2012-02-08
K092897LAP LOOPMedsys, S.A.2010-02-01
K070315LINA LOOP, MODELS: EL-160-4, EL-160-8, EL-200-4, EL-200-8Lina Medical Aps2007-10-30
K022979LAPARETTE, MODEL LAP J L S H NInstruments Medicaux G.B., Inc.2002-12-18
K010752AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGYAesculap, Inc.2001-06-11
K003405ENDOSCOPIC MONOPOLAR FORCEPS-SCISSORS, EMF-2000 TO 2999,ENDOSCOPICS MONOPOLARFOEPS-GRASPERS, EMF-3000 TO 3999, ENDOSCOPOHighland / Marietta, Inc.2001-05-07

Legacy Summary#

summary

FDA Review#

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