FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ELECTROSURGICAL HEMOSTATIC FORCEPS SERIES

K Number: K062517 · Decision Dec 22, 2006
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
45
Applicant Total
81
Review Days
116

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Basic Information

Device Name
ELECTROSURGICAL HEMOSTATIC FORCEPS SERIES
K Number
K062517
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Olympus Medical Systems Corporation
Date Received
August 28, 2006
Decision Date
December 22, 2006
Product Code
KGE
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KGE Forceps, Biopsy, Electric

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K Number Device Name
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K252889 Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M)
K250409 Disposable Balloon Catheter (B5-2Q); Disposable Balloon Catheter (B7-2Q); Disposable Balloon Catheter (B7-2LA)
K252247 Injector Force Max Single Use Injector (NM-400L); Injector Force Max Single Use Injector (NM-400U); Injector Force Max Single Use Injector (NM-400Y); Injector Force Max Single Use Injector (NM-401L)
K250351 Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife (KD-620UR); Single Use Electrosurgical Knife (KD-650L, KD-650U)
K252150 Ultrasonic Bipolar Generator (USG-410); Reuseable Cordless Transducer (TD-410); THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 45cm (TB2-0545FC); THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 35cm (TB2-0535FC); THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 25cm (TB2-0525FC); THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 20cm (TB2-0520FC)
K250187 Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U)
K251859 EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)
K251986 AUXILIARY WATER TUBE MAJ-855
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