510(k) K992996

Device
ENABLE ENDOSCOPIC BIPOLAR SCISSORS
Applicant
ENABLE MEDICAL CORP.
510(k) number
K992996
Product code
GEI  
Decision
Substantially Equivalent (SESE)
Decision date
1999-11-24
Date received
1999-09-07
Regulation
878.4400
Classification name
Electrosurgical, Cutting & Coagulation & Accessories
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
MARK L FRIEDMAN
Address
6345 Centre Park Dr. West Chester OH US 45069 45069

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code GEI  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K253918Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St)F Care Systems USA, LLC2026-06-02
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K261202ENTire IRE SystemEntire Medical , Ltd.2026-05-29
K252833VIVA combo RF SystemStarmed Co., Ltd.2026-05-26
K253134LAGIS Endoscopic Instruments- Scissors (EI-330S EI-330S-T EI-330MS EI-330MS-T)Lagis Enterprise Co., Ltd.2026-05-20
K260522RhinAer+ StylusAerin Medical, Inc.2026-05-18
K253917ARION ARC SystemPlasma Surgical, Inc.2026-04-10
K253777Ascblue (8010)Ascblue Corporation2026-04-10
K260466Multifunctional Operational Dissectors (Electrosurgical Pencils);Multifunctional Operational Dissectors (Disposable Electrode)Zhejiang shuyou Surgical Instrument Co., Ltd.2026-04-07
K260397SYNERJET PRO (SP-1002); InPhiuse (SP-1002); WOWJET (SP-1002)Hironic Co., Ltd.2026-04-06
K253405Prana SystemPrana Surgical2026-04-01
K254122FLOW FLEXTEND Wand (72290039)ArthroCare Corporation2026-03-30
K260255AVENTIX PFX System (PFX01); NOVOCLEAR Device (CLR001)Aventix Medical, Inc.2026-03-27
K253680LYNX COBLATION Laryngeal Wand (72290254)ArthroCare Corporation2026-03-25

Legacy Summary#

summary

FDA Review#

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