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

GIP/MEDI-GLOBE POLYPECTOMY SNARES

K Number: K943935 · Decision May 26, 1995
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
62
Applicant Total
18
Review Days
287

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Basic Information

Device Name
GIP/MEDI-GLOBE POLYPECTOMY SNARES
K Number
K943935
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
August 12, 1994
Decision Date
May 26, 1995
Product Code
FDI
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
FDI Snare, Flexible

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Other Clearances by Medi-Globe Corp.

K Number Device Name
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K011261 STONE EXTRACTOR BALLOON CATHETER
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
K953355 GIP/MEID-GLOBE HOT BIOPSY FORCEPS
K955558 GIP/MEDI-GLOBE SCLEROTHERAPY NEEDLES
K953827 GIP/MEDI-GLOBE ERCP CATHETERS
K941973 GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES
Search all 18 clearances from Medi-Globe Corp. →