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

XUES-41 ENDOSCOPIC ELECTROSURGICAL UNIT

K Number: K030194 · Decision Mar 24, 2003
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
187
Applicant Total
22
Review Days
62

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Basic Information

Device Name
XUES-41 ENDOSCOPIC ELECTROSURGICAL UNIT
K Number
K030194
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Olympus Optical Co.
Date Received
January 21, 2003
Decision Date
March 24, 2003
Product Code
KNS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
Y

Classifications

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

Product Code Device Name
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)

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Other Clearances by The Olympus Optical Co.

K Number Device Name
K032066 SONOSURG SYSTEM
K021962 OLYMPUS ULTRASONIC SURGICAL SYSTEM
K023984 MODIFICATION TO OLYMPUS BRONCHOSCOPES BF-40 SERIES, BF-240 SERIES, AND BF-160 SERIES
K023272 DISPOSABLE ASPIRATION NEEDLE NA-200H
K023767 UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES
K012074 XBO1-824-18/19/20 BIOPSY FORCEPS
K012073 OLYMPUS SPRAY CATHETER PW-6C-1
K011869 XENF-DP RHINO-LARYNGOFIBERSCOPE, ITS ACCESSORIES AND ANCILLARY EQUIPMENT
K011149 DISPOSABLE BENDING CANNULA PR-233Q
K011151 EVIS EXERA GASTROINTESTINAL VIDEOSCOPE GIF-Q160Z
Search all 22 clearances from The Olympus Optical Co. →