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

MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST, ALPHA RT AND ALPHA IQ

K Number: K981641 · Decision Jul 17, 1998
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
20
Review Days
70

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Basic Information

Device Name
MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST, ALPHA RT AND ALPHA IQ
K Number
K981641
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Instrumentarium Corp.
Date Received
May 8, 1998
Decision Date
July 17, 1998
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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