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

LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM

K Number: K841732 · Decision Jun 5, 1984
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
9
Applicant Total
37
Review Days
40

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Basic Information

Device Name
LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM
K Number
K841732
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1870
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Sybron Corp.
Date Received
April 26, 1984
Decision Date
June 5, 1984
Product Code
IZP
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
IZP Programmer, Changer, Film/Cassette, Radiographic

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Other Clearances by Sybron Corp.

K Number Device Name
K862284 SEALITE
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K842132 TYCOS SELF-CHECK/DIGITAL FEVER THERMO
K841910 KERR SEALAPEX ROOT CANAL SEALER
K840469 TYCOS SELF CHECK BPM3 BLOOD PRESS MONI
K840407 KERR RESIN BONDED BRIDGE CEMENT
K840607 LF MOTORIZED RADIOGRAPHIC FILM VIEWER
K833138 DIGITAL INJECTOR SYS
K823795 EVERBOND GLASS IONOMER CEMENT
Search all 37 clearances from Sybron Corp. →