Atlas FDA

FDR IMAGE STITCHING OPTION

FDA 510(k) clearance K101686 · decided 2010-10-29

Clearance details

K-number
K101686
Device name
FDR IMAGE STITCHING OPTION
Applicant
Fujifilm Medical System U.S.A., Inc.
Decision
Substantially Equivalent
Date received
2010-06-16
Decision date
2010-10-29
Days to decision
135 days
Clearance type
Special
Product code
KPR
Device class
2
Regulation number
892.1680
Medical specialty
Radiology
Advisory committee
Radiology
Location
Stamford, CT, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
FULL FIELD DIGITAL MAMMOGRAPHY (P050014/S002)Fujifilm Medical System U.S.A., Inc.2009-08-11
FUJI COMPUTED RADIOGRAPHY MAMMOGRAPHY SUITE (P050014/S001)Fujifilm Medical System U.S.A., Inc.2009-01-09
FUJI'S COMPUTED RADIOGRAPHY MAMMOGRAPHY SUITE (FCRMS) (P050014)Fujifilm Medical System U.S.A., Inc.2006-07-10