ClearanceBrief
Company ยท DE

Medelec , Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 1997. 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
GWFStimulator, Electrical, Evoked Response2
GWQFull-Montage Standard Electroencephalograph2
OLTNon-Normalizing Quantitative Electroencephalograph Software2
BSZGas-Machine, Anesthesia1
GWJStimulator, Auditory, Evoked Response1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 20, 1997K965065TECA. MILLENNIUM
Medelec , Ltd., GB
GWF
Jan 27, 1997K964280DG NERVUS
Medelec , Ltd., DE
GWQ
Jan 17, 1996K954157DG PORTABLE SYSTEM
Medelec , Ltd., DE
OLT
Nov 8, 1995K953799DG EXAMINER PLUS
Medelec , Ltd., DE
OLT
Oct 19, 1995K953732TECA PREMIERE
Medelec , Ltd., DE
GWJ
May 25, 1994K934670DG 3P SYSTEM
Medelec , Ltd., DE
GWQ
Apr 26, 1994K934669ARC
Medelec , Ltd., GB
BSZ
Nov 24, 1992K923303SAPPHIRE PREMIERE
Medelec , Ltd., GB
GWF

Latest recalls

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