Medical Device Manufacturer · US , Danbury , CT

Lorad Corp. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1994

Recent clearances: LORAD 1-650 (INTERNATIONAL 650), LITE TOUCH ERBIUM LASER TREATMENT SYSTEM, LORAD M-III ELITE (M-III E)

Total

Cleared

Denied

Lorad Corp. has 12 FDA 510(k) cleared radiology devices. Based in Danbury, US.

Historical record: 12 cleared submissions from 1994 to 1999.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Lorad Corp. is one of 8125 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Lorad Corp.

12 devices

1-12 of 12

Cleared Sep 03, 1999

LORAD 1-650 (INTERNATIONAL 650)

K992280 · IZH

Radiology · 58d

Cleared Jan 16, 1998

LITE TOUCH ERBIUM LASER TREATMENT SYSTEM

K974460 · GEX

General & Plastic Surgery · 52d

Cleared Dec 23, 1997

LORAD M-III ELITE (M-III E)

LORAD M-IV, LORAD M-IVI

K945241 · IZH

Radiology · 155d

Cleared Mar 02, 1995

DIGITAL SPOT MAMMOGRAPHY FOR STEROTACTIC APPLICATION

K950608 · IZH

Radiology · 21d

Cleared Dec 27, 1994

MAMMOGRAPHIC X-RAY UNIT

LORAD M-IIE MODIFICATION

Lorad Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Lorad Corp.

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