ClearanceBrief
Company ยท DE

Somnomedics GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2024. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MNRVentilatory Effort Recorder4
OLVStandard Polysomnograph With Electroencephalograph2
DSHRecorder, Magnetic Tape, Medical1
GYBMedia, Electroconductive1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 8, 2024K240700HomeSleepTest (HST, HST REM+)
Somnomedics GmbH, DE
OLV
Nov 27, 2023K231104ABPMpro
Somnomedics GmbH, DE
DSH
Jun 15, 2022K212325EEG-acp
Somnomedics GmbH, DE
GYB
Aug 12, 2020K201054SOMNOscreen plus
Somnomedics GmbH, DE
OLV
Jan 30, 2015K140861SOMNOTOUCH RESP
Somnomedics GmbH, DE
MNR
Sep 18, 2008K081485SOMNOWATCH
Somnomedics GmbH
MNR
Jul 18, 2007K071556SOMNOSCREEN EEG10-20
Somnomedics GmbH
MNR
Jan 24, 2007K060708SOMNOSCREEN
Somnomedics GmbH & Co. KG
MNR

Latest recalls

DateFirm and productCodeLinked 510(k)
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