Atlas FDA

E.CAM COMPUTER

FDA 510(k) clearance K992731 · decided 1999-11-10

Clearance details

K-number
K992731
Device name
E.CAM COMPUTER
Applicant
Siemens Medical Solutions USA, Inc.
Decision
Substantially Equivalent
Date received
1999-08-13
Decision date
1999-11-10
Days to decision
89 days
Clearance type
Traditional
Product code
KPS
Device class
2
Regulation number
892.1200
Medical specialty
Radiology
Advisory committee
Radiology
Location
Hoffman Estates, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
e.cam -emission computed tomography system Used to detect or image the distribution of rad recall (Z-0914-2015)Siemens Medical Solutions USA, Inc.2015-01-06

PMA approvals by this applicant

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MAMMOMAT Revelation with Tomosynthesis Option System (P140011/S007)Siemens Medical Solutions USA, Inc.2020-08-21
MAMMOMAT Revelation with Tomosynthesis Option (P140011/S006)Siemens Medical Solutions USA, Inc.2019-12-10
Mammomat Inspiration with Tomosynthesis Option / Mammomat Revelation with Tomosynthesis Option (P140011/S005)Siemens Medical Solutions USA, Inc.2017-09-29
MAMMOMAT INSPIRATION WITH TOMOSYNTHESIS OPTION (P140011/S003)Siemens Medical Solutions USA, Inc.2017-03-23
MAMMOMAT INSPIRATION WITH TOMOSYNTHESIS OPTION (P140011/S001)Siemens Medical Solutions USA, Inc.2016-05-12
MAMMOMAT INSPIRATION TOMOSYNTHESIS OPTION (P140011/S002)Siemens Medical Solutions USA, Inc.2016-01-13
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