Home › Device types › LMC
Camera, Multi Format, Radiological
FDA product code LMC · Class 2 · Radiology
73
Registered devices
6
Adverse events
3
Recalls
121
510(k) clearances
Devices with this code
Codonics Horizon® G1 Multi-media Imager — CODONICS INC.Codonics Horizon® Operating Software — CODONICS INC.Codonics Horizon® SF Multi-media Imager — CODONICS INC.FUJI MEDICAL DRY FILM — FUJIFILM CORPORATIONDrystar 5302 — AGFADRYPIX Plus — FUJIFILM CORPORATIONDRYPRO SIGMA 2 — KONICA MINOLTA, INC.DRYPRO MODEL 832 — KONICA MINOLTA, INC.SONY — SONY CORPORATIONFUJI MEDICAL DRY FILM — FUJIFILM CORPORATIONDRYPRO MODEL 873 — KONICA MINOLTA, INC.Codonics Horizon® G2 Multi-media Imager — CODONICS INC.Film Tray — FUJIFILM CORPORATIONFUJI MEDICAL DRY FILM — FUJIFILM CORPORATIONFUJI MEDICAL DRY FILM — FUJIFILM CORPORATIONCodonics Horizon® Multi-media Imager — CODONICS INC.DRYPIX Smart — FUJIFILM CORPORATIONDRYVIEW 5700 Laser Imaging System — CARESTREAM HEALTH, INC.FUJI MEDICAL DRY FILM — FUJIFILM CORPORATIONFUJI MEDICAL DRY FILM — FUJIFILM CORPORATIONDRYPRO SIGMA — KONICA MINOLTA, INC.Magazine L — FUJIFILM CORPORATIONFUJI MEDICAL DRY FILM — FUJIFILM CORPORATIONDRYVIEW 5950 Laser Imaging System — CARESTREAM HEALTH, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-03-11 | Philips Medical Systems (Cleveland) Inc | The firm was notified by a customer that the collimator exchange carriage and the collimator storage cabinet were misaligned. |
| 2008-05-16 | AGFA Corp. | The "Film Calibration" setting on the printers was set to the default "OFF" position instead of "ON". |
| 2003-11-25 | AGFA Corp. | The GS1 circuit board may fail resulting in smoke or fire. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.