ClearanceBrief
Company ยท US

Lorad Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1999. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IZHSystem, X-Ray, Mammographic11
GEXPowered Laser Surgical Instrument1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 3, 1999K992280LORAD 1-650 (INTERNATIONAL 650)
Lorad Corp.
IZH
Jan 16, 1998K974460LITE TOUCH ERBIUM LASER TREATMENT SYSTEM
Lorad Corp.
GEX
Dec 23, 1997K973631LORAD M-III ELITE (M-III E)
Lorad Corp.
IZH
Jul 24, 1995K952210LORAD STEROLOC II
Lorad Corp.
IZH
Mar 31, 1995K945241LORAD M-IV, LORAD M-IVI
Lorad Corp.
IZH
Mar 2, 1995K950608DIGITAL SPOT MAMMOGRAPHY FOR STEROTACTIC APPLICATION
Lorad Corp.
IZH
Dec 27, 1994K945496MAMMOGRAPHIC X-RAY UNIT
Lorad Corp.
IZH
Dec 14, 1994K945272RHODIUM FILTER
Lorad Corp.
IZH
Oct 14, 1994K934868LORAD TRANSPO
Lorad Corp.
IZH
Jan 31, 1994K934870LORAD D-550
Lorad Corp.
IZH
Jan 31, 1994K934748LORAD M-IIE MODIFICATION
Lorad Corp.
IZH
Jan 28, 1994K934625LORAD M-III
Lorad Corp.
IZH

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes