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

MINXRAY 500M MAMMOGRAPHIC SYSTEM

K Number: K854510 · Decision Jan 1, 1986
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
18
Review Days
50

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Basic Information

Device Name
MINXRAY 500M MAMMOGRAPHIC SYSTEM
K Number
K854510
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Minxray, Inc.
Date Received
November 12, 1985
Decision Date
January 1, 1986
Product Code
IZH
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
IZH System, X-Ray, Mammographic

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Other Clearances by Minxray, Inc.

K Number Device Name
K210479 IMPACT and X-Ranger
K201575 CMDR 2C (Multiple Models)
K191451 CMDR 2CW (Multiple models)
K182207 TR90BH
K171353 CMDR 2ST (Multiple Models), CMDR 2SPE (Multiple Models), Integris
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
Search all 18 clearances from Minxray, Inc. →