FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

STYROFOAM CUTTERS FOR BLOCK CASTING SYSTEM

K Number: K010062 · Decision Mar 13, 2001
Classifications
1
FEI Numbers
123
Registration Numbers
124
Same Product Code
717
Applicant Total
9
Review Days
64

Basic Information

Device Name
STYROFOAM CUTTERS FOR BLOCK CASTING SYSTEM
K Number
K010062
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ARPLAY MEDICAL S.A.
Date Received
January 8, 2001
Decision Date
March 13, 2001
Product Code
IYE
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IYE Accelerator, Linear, Medical

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K Number Device Name
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K003779 IMMOBILIZATION SYSTEM FOR ENT
K003778 BREAST-BOARD (MULTIPLE)
K010172 LEAD BLOCKS
K010174 TRAY ADAPTERS, MULTIPLE
K010063 COUCH FOR TOTAL BODY RADIATION
K004015 BEAM BLOCK TRAYS