ClearanceBrief
Company ยท US

Mennen Greatbatch Electonics

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1977. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DPSElectrocardiograph1
DRGTransmitters And Receivers, Physiological Signal, Radiofrequency1
DRQAmplifier And Signal Conditioner, Transducer Signal1
DXJDisplay, Cathode-Ray Tube, Medical1
GWQFull-Montage Standard Electroencephalograph1
KXNMonitor, Cardiac, Fetal1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 22, 1977K772000ECG TELEMETRY SYSTEM
Mennen Greatbatch Electonics
DRG
Jun 3, 1977K770832PORTASCOPE II
Mennen Greatbatch Electonics
DPS
Feb 24, 1977K770279MONITOR, PORTABLE, PART #431-010
Mennen Greatbatch Electonics
DXJ
Feb 14, 1977K770247D.C. AMPLIFIER MODULE
Mennen Greatbatch Electonics
DRQ
Feb 14, 1977K770246ISOLATED EEG AMPLIFIER MODULE
Mennen Greatbatch Electonics
GWQ
Feb 14, 1977K770245ABDOMINAL FETAL ECG MODULE
Mennen Greatbatch Electonics
KXN

Latest recalls

DateFirm and productCodeLinked 510(k)
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