ClearanceBrief
Company ยท US

Topera, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2011 to 2015. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DQKComputer, Diagnostic, Programmable5
MTDCatheter, Intracardiac Mapping, High-Density Array2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 15, 2015K151245Rhythm View Workstation (non-streaming, steaming option)
Topera, Inc.
DQK
Dec 19, 2014K142901RhythmView Workstation
Topera, Inc.
DQK
Sep 9, 2014K142182FRIMAP ADAPTER CONNECTOR (MAC)
Topera, Inc.
MTD
Dec 16, 2013K133305RHYTHM VIEW WORKSTATION
Topera, Inc.
DQK
Oct 31, 2013K130827FIRMAP CATHETER
Topera, Inc.
MTD
Apr 24, 2013K123295RHYTHM VIEW
Topera, Inc.
DQK
Sep 23, 2011K110878RHYTHMVIEW (TM)
Topera, Inc.
DQK

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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