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

CMDR 2C (Multiple Models)

K Number: K201575 · Decision Jul 8, 2020
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
18
Review Days
27

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Basic Information

Device Name
CMDR 2C (Multiple Models)
K Number
K201575
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1720
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Minxray, Inc.
Date Received
June 11, 2020
Decision Date
July 8, 2020
Product Code
IZL
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
IZL System, X-Ray, Mobile

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K Number Device Name
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K153059 HF1202H PowerPlus Portable X-ray Equipment
K141885 CMDR-2ST & CMDR-2SLWT DIGITAL PORTABLE X-RAY
K091255 MINXRAY, MODEL: BPD60
K100449 MINXRAY MODEL CMDR-2S
K082627 MINXRAY, MODEL CMDR-1S AND CMDR-1S-MIL
K052721 MINXRAY, MODEL HF100H+
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