ClearanceBrief
Company ยท DE

Corscience GmbH & Co. KG

FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2020. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DPSElectrocardiograph1
DXHTransmitters And Receivers, Electrocardiograph, Telephone1
GWQFull-Montage Standard Electroencephalograph1
HCCDevice, Biofeedback1
OLUNormalizing Quantitative Electroencephalograph Software1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 30, 2020K193159NeuroAmp II, NeuroAmp II.5s
Corscience GmbH & Co. KG, DE
GWQ
Dec 28, 2018K183369COR12 ECG
Corscience GmbH & Co., DE
DPS
Mar 9, 2012K112077HBIDB - HUMAN BRIAN INDEX SOFTWARE
Corscience GmbH & Co. KG
OLU
Sep 2, 2008K082077BT3/6, BT12
Corscience GmbH & Co. KG
DXH
Feb 28, 2008K073557EEG NEUROAMP, MODEL CS10137
Corscience GmbH & Co. KG, DE
HCC

Latest recalls

DateFirm and productCodeLinked 510(k)
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