ClearanceBrief
Company ยท US

Med USA

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1995. 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
KQGInstrument, Coagulation2
EAKScreen, Leaded, Operator Radiation Protector1
GKLCounter, Cell, Automated (Particle Counter)1
GXYElectrode, Cutaneous1
KFZHumidifier, Non-Direct Patient Interface (Home-Use)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 11, 1995K944445ED CORP RADIATION SCREEN
Med Corp.
EAK
Mar 14, 1990K896766TD-28 DISPOSABLE ELECTRODE
Med USA
GXY
Sep 29, 1986K862047COAGULATOR (8 CHANNEL)
Med USA
KQG
Aug 13, 1985K852492COAGULATOR
Med USA
KQG
Jun 5, 1985K850711INHALATION THERAPY NEBULIZER DEVICE
Med USA
KFZ
Feb 25, 1985K841803A1 SYSTEME 8201/2
Med USA
GKL

Latest recalls

DateFirm and productCodeLinked 510(k)
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