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

PHT-6500, PHT-60CFO

K Number: K130432 · Decision May 31, 2013
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
40
Review Days
99

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Basic Information

Device Name
PHT-6500, PHT-60CFO
K Number
K130432
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VATECH Co., Ltd.
Date Received
February 21, 2013
Decision Date
May 31, 2013
Product Code
OAS
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
OAS X-Ray, Tomography, Computed, Dental

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Other Clearances by VATECH Co., Ltd.

K Number Device Name
K260093 Green X 12 VE (PHT-70CHS); Green X VE (PHT-70CHS)
K243088 Green X 12 SE (PHT-40CHS)
K243081 Green X 21 (PHT-90CHO)
K240040 VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)
K231796 Grreen X 12 (Model: PHT-75CHS)
K223058 EzRay Air 2 Wall (Model: VEX-S350W)
K213462 EzRay M18 (Model: VMX-P400)
K210329 Green X 18(Model : PHT-75CHS)
K203667 EzRay M (Model: VMX-P300)
K203797 vatech A9 (Model : PHT-30CSS)
Search all 40 clearances from VATECH Co., Ltd. →