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

ULTRACLIP II WING AND ULTRACLIP II COIL

K Number: K063238 · Decision Jan 30, 2007
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
109
Applicant Total
11
Review Days
96

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Basic Information

Device Name
ULTRACLIP II WING AND ULTRACLIP II COIL
K Number
K063238
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Inrad
Date Received
October 26, 2006
Decision Date
January 30, 2007
Product Code
NEU
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
NEU Marker, Radiographic, Implantable

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NEU), ordered by most recent decision date.

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Other Clearances by Inrad

K Number Device Name
K093399 PRECISECORE 10 MM BIOPSY DEVICE- 14GA X 5 CM MODEL 670514, 671014, 670518 671018, 670520
K093256 SELECTCORE VARIABLE THROW BIOPSY DEVICE MODEL 991014, 991514, 991018, 991518, 992018
K090611 REVOLUTION FULL CORE BIOPSY
K042341 ULTRACLIP II US
K041201 ULTRACLIP II MR
K000612 ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE
K993785 ULTRACLIP TISSUE MARKER
K981721 C0-AXIAL INTRODUCER NEEDLE
K981166 ACCUCORE CORE BIOPSY NEEDLE CATALOG CODES:581014, 581614, 581618, 582018, 582518, 581620, 582020, 581214
K980587 IV DECANTER-FLEXIBLE
Search all 11 clearances from Inrad →