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

GIP/MEID-GLOBE HOT BIOPSY FORCEPS

K Number: K953355 · Decision Apr 4, 1996
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
45
Applicant Total
18
Review Days
262

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Basic Information

Device Name
GIP/MEID-GLOBE HOT BIOPSY FORCEPS
K Number
K953355
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medi-Globe Corp.
Date Received
July 17, 1995
Decision Date
April 4, 1996
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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K010714 EXPANDER, MODELS 1400880, 1401280, 1401680, 1401880, 1410420, 1410620, 1410830
K010549 BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS)
K990220 MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM
K955558 GIP/MEDI-GLOBE SCLEROTHERAPY NEEDLES
K953827 GIP/MEDI-GLOBE ERCP CATHETERS
K941973 GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES
K943935 GIP/MEDI-GLOBE POLYPECTOMY SNARES
Search all 18 clearances from Medi-Globe Corp. →