ClearanceBrief
Company ยท US

Rms Div.

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1996. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IXLDevice, Spot-Film2
IXRTable, Radiographic, Tilting2
CCWLaryngoscope, Rigid1
EIXProbe, Periodontic1
EJSAlloy, Other Noble Metal1
EJTAlloy, Gold-Based Noble Metal1
HTYPin, Fixation, Smooth1
IZZTable, Radiographic, Non-Tilting, Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 30, 1996K963367RMS K-WIRE
Rms Div.
HTY
Dec 29, 1995K954438SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE
Rms Div.
CCW
Dec 14, 1994K944848THE VIVACARE T.P.S. PROBE
Rms Div.
EIX
Nov 3, 1994K944557DW250 #91
Rms Div.
EJT
Jun 22, 1994K941625DW234 #29
Rms Div.
EJS
Aug 1, 1990K902403ELITE R/F SPOT FILM DRIVE
Rms Div.
IXL
May 31, 1990K902146SFD-035 SPOT FILM DEVICE
Rms Div.
IXL
Jan 22, 1990K896665EXT-600 TABLE, RADIOGRAPHIC, ELEVATING
Rms Div.
IZZ
Nov 27, 1989K896119RMS 90/15 RADIOGRAPHIC/FLUOROSCOPIC TILTING TABLE
Rms Div.
IXR
Nov 21, 1989K896324ELITE 1500 RADIOGRAPHIC TILTING TABLE
Rms Div.
IXR

Latest recalls

DateFirm and productCodeLinked 510(k)
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