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

FLUOROPLUA CARDIAC AND/OR INSTAVIEW

K Number: K941917 · Decision Feb 24, 1995
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
8
Review Days
311

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Basic Information

Device Name
FLUOROPLUA CARDIAC AND/OR INSTAVIEW
K Number
K941917
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Fidelity Medical, Inc.
Date Received
April 19, 1994
Decision Date
February 24, 1995
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

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Other Clearances by Fidelity Medical, Inc.

K Number Device Name
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K903774 LP-PLUS
K872928 LP-3000 HIGH RESOLUTION ELECTROCARDIOGRAPH
K864614 LP-3 ELECTROCARDIOGRAPH
K841780 CLINICAL ELECTRONIC THERMOMETER