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

AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA CURIX AND LIGHTWEIGHT CASSETTE

K Number: K023020 · Decision Sep 26, 2002
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
50
Applicant Total
19
Review Days
15

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Basic Information

Device Name
AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA CURIX AND LIGHTWEIGHT CASSETTE
K Number
K023020
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1850
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Agfa Corp.
Date Received
September 11, 2002
Decision Date
September 26, 2002
Product Code
IXA
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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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K050810 AGFA CR50.0
K042779 RADIOTHERAPY SOLUTION BASED ON CR
K041701 AFGA CR25.0 COMPUTED RADIOGRAPHY SYSTEM
K040555 IMPAX CLIENT EMBRACE
K040344 IMPAX OT3000 ORTHOPEDIC WORKSTATION
K032635 DRYSTAR 5300 MEDICAL IMAGE PRINTER, MODEL 5300
K023287 DRYSTAR 5500
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