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

SONOTIP II ULTRASOUND NEEDLE SYSTEM

K Number: K051247 · Decision Jun 16, 2005
Classifications
1
FEI Numbers
128
Registration Numbers
128
Same Product Code
132
Applicant Total
18
Review Days
31

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Basic Information

Device Name
SONOTIP II ULTRASOUND NEEDLE SYSTEM
K Number
K051247
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medi-Globe Corp.
Date Received
May 16, 2005
Decision Date
June 16, 2005
Product Code
FCG
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
FCG Biopsy Needle

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Other Clearances by Medi-Globe Corp.

K Number Device Name
K061222 INJECTRA INJECTION NEEDLE
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
K943935 GIP/MEDI-GLOBE POLYPECTOMY SNARES
Search all 18 clearances from Medi-Globe Corp. →