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

MAMMOTEST ADAPTER DRIVER

K Number: K973400 · Decision Nov 10, 1997
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
175
Applicant Total
69
Review Days
62

Basic Information

Device Name
MAMMOTEST ADAPTER DRIVER
K Number
K973400
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
FISCHER IMAGING CORP.
Date Received
September 9, 1997
Decision Date
November 10, 1997
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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