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

DOSE VERIFICATION SYSTEM

K Number: K052118 · Decision Apr 3, 2006
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
91
Applicant Total
7
Review Days
242

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Basic Information

Device Name
DOSE VERIFICATION SYSTEM
K Number
K052118
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sicel Technologies, Inc.
Date Received
August 4, 2005
Decision Date
April 3, 2006
Product Code
LHN
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
LHN System, Radiation Therapy, Charged-Particle, Medical

Similar 510(k) Clearances

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

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Other Clearances by Sicel Technologies, Inc.

K Number Device Name
K083035 DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM
K081859 MODIFICATION TO ONEDOSE PATIENT DOSIMETRY SYSTEM
K080004 DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM
K071399 DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODEL DVS-I-11: DVS INSERTION TOOL, DVS-D-A: DVS DOSIMETER, DVS-R-100
K061051 DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODELS DVS-I-11, DVS INSERTION TOOL, DVS-D-A, DVS DOSIMETER
K040687 ONEDOSE PATIENT DOSIMETRY SYSTEM