Atlas FDA

IMPAX CLIENT EMBRACE

FDA 510(k) clearance K040555 · decided 2004-05-26

Clearance details

K-number
K040555
Device name
IMPAX CLIENT EMBRACE
Applicant
Agfa Corp.
Decision
Substantially Equivalent
Date received
2004-03-02
Decision date
2004-05-26
Days to decision
85 days
Clearance type
Traditional
Product code
LLZ
Device class
2
Regulation number
892.2050
Medical specialty
Radiology
Advisory committee
Radiology
Location
Waterloo, Ontario, CA
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
IMPAX 4.1, IMPAX 4.5, IMPAX 5.0, IMPAX 5.1 IMPAX 5.2, IMPAX 6.0, IMPAX 6.2; Picture Archiv recall (Z-1243-2008)AGFA Corp.2008-09-11
WEB1000 Versions 3.1, 4.1 and 5.1, Picture Archiving and Communications systems (PACs), us recall (Z-1244-2008)AGFA Corp.2008-09-11
IMPAX 6.2.1 System, Picture Archiving and Communications system (PAC), used in the accepta recall (Z-1245-2008)AGFA Corp.2008-09-11