FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

VIEW ARCHIVING STATION

K Number: K971176 · Decision Sep 3, 1997
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
198
Applicant Total
23
Review Days
156

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Basic Information

Device Name
VIEW ARCHIVING STATION
K Number
K971176
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1600
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Electromed Intl., Ltd.
Date Received
March 31, 1997
Decision Date
September 3, 1997
Product Code
IZI
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
IZI System, X-Ray, Angiographic

Similar 510(k) Clearances

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Other Clearances by Electromed Intl., Ltd.

K Number Device Name
K003688 VIEW READING STATION
K000474 VIEW NT
K990759 VIEW COM
K974255 CD-R STATION AND VRS-2000
K950694 COMPACT-X
K880050 EDEC 60R
K875341 EDEC 60 R/F
K875342 EDEC 90C
K871145 EDEC 50C CONSTANT POTENTIAL X-RAY GENERATOR
K870851 EDEC 80 CONSTANT POTENTIAL X-RAY GENERATOR
Search all 23 clearances from Electromed Intl., Ltd. →