FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

CARDIOSCINT (LEFT VENTRICULAR FUNCTION MONITOR)

K Number: K902460 · Decision Aug 28, 1990
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
29
Applicant Total
8
Review Days
85

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Basic Information

Device Name
CARDIOSCINT (LEFT VENTRICULAR FUNCTION MONITOR)
K Number
K902460
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1320
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Oakfield Instruments, Ltd.
Date Received
June 4, 1990
Decision Date
August 28, 1990
Product Code
IZD
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
IZD Probe, Uptake, Nuclear

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Other Clearances by Oakfield Instruments, Ltd.

K Number Device Name
K964804 FLEXILOG LS
K964589 FLEXILOG 3000
K961895 FLEXILOG LS 13921
K945069 FLEXILOG 2000
K920115 MEDISCINT
K896288 FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM
K894902 SOURCERER