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

DIGITAL DIAGNOSTIC X-RAY SYSTEM, MODELS MAK 1500, MAK 2000 AND MAK 3000

K Number: K082798 · Decision Oct 28, 2008
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
9
Review Days
35

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Basic Information

Device Name
DIGITAL DIAGNOSTIC X-RAY SYSTEM, MODELS MAK 1500, MAK 2000 AND MAK 3000
K Number
K082798
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicatech USA
Date Received
September 23, 2008
Decision Date
October 28, 2008
Product Code
KPR
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
KPR System, X-Ray, Stationary

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Other Clearances by Medicatech USA

K Number Device Name
K230918 MasterX 800 Series
K190601 MasteRad MX30
K143257 KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic System
K130377 KRYSTALRAD NEW SERIESDIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM
K112132 KRYSTALRAD 660 DIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM
K102285 KRYSTALRAD (ATAL8)
K102284 KRYSTALRAD 560 (FLAATZ 560)
K080582 MEDICATECH, MODEL DDR MAK-800, DDT MAK-1000 FS, DDR MAK-1100 FA