FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FUJI CR IMAGING PLATE

K Number: K862414 · Decision Feb 26, 1987
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
34
Applicant Total
14
Review Days
246

Basic Information

Device Name
FUJI CR IMAGING PLATE
K Number
K862414
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1960
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
PAREXEL INTL. CORP.
Date Received
June 25, 1986
Decision Date
February 26, 1987
Product Code
EAM
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
EAM Screen, Intensifying, Radiographic

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K862415 TYPE 633 COMPUTED RADIOGRAPHY (CR) FILM
K853295 EMODREN EXCHANGEABLE PLASTIC BELLOWS
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