Atlas FDA

POLYSTAR ANGIOGRAPHIC X-RAY SYSTEM

FDA 510(k) clearance K913120 · decided 1991-08-16

Clearance details

K-number
K913120
Device name
POLYSTAR ANGIOGRAPHIC X-RAY SYSTEM
Applicant
Siemens Medical Solutions USA, Inc.
Decision
Substantially Equivalent
Date received
1991-07-15
Decision date
1991-08-16
Days to decision
32 days
Clearance type
Traditional
Product code
IZI
Device class
2
Regulation number
892.1600
Medical specialty
Radiology
Advisory committee
Radiology
Location
Iselin, NJ, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
POLYSTAR, Angiographic X-Ray System, Model 1148902 recall (Z-0195-05)Siemens Medical Solutions USA, Inc2004-11-16
POLYSTAR T.O.P., Angiographic X-Ray System, Model Numbers 1148902 and 4784505. recall (Z-0196-05)Siemens Medical Solutions USA, Inc2004-11-16

PMA approvals by this applicant

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MAMMOMAT B.brilliant with Tomosynthesis Option (P140011/S008)Siemens Medical Solutions USA, Inc.2024-09-23
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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