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

L-F/KODAK FLEXIBLE GRID CASSETTE

K Number: K883312 · Decision Aug 16, 1988
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
50
Applicant Total
27
Review Days
11

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Basic Information

Device Name
L-F/KODAK FLEXIBLE GRID CASSETTE
K Number
K883312
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1850
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Mallinckrodt Group, Inc.
Date Received
August 5, 1988
Decision Date
August 16, 1988
Product Code
IXA
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
IXA Cassette, Radiographic Film

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K920742 HYDRAJUST IV UROLOGICAL TABLE
K912944 CT 8000 DIGITAL INJECTION SYSTEM
K913264 HYDRAVIEW 1000 DIGITAL IMAGE PROCESS/STOR DEVICE
K905789 FRANKLIN 9000 WALL STAND
K904147 HUGH YOUNG II UROLOGICAL X-RAY SYSTEM
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