Medicor USA , Ltd.
Medicor USA , Ltd. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1986.
Top product codes for Medicor USA , Ltd.
Recent clearances by Medicor USA , Ltd.
- K861994 — MODEL RS-3I RADIOGRAPHIC/FLUROSCOPIC X-RAY SYSTEM
- K861995 — MODEL RS-3 RADIOGRAPHIC STAND
- K860025 — MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR
- K850761 — MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C
- K851358 — MODEL BION 2/TYPE 90 ROOM IONIZER
- K851094 — MODEL BION 1/TYPE 1084T CAR IONIZER
- K843335 — FLOOR MOUNTED X-RAY TUBESTAND
- K840227 — UROLIX-3 UROLOGICAL TABLE
- K840225 — C-ARM CEILING CRANE FT-2
- K840226 — MOTOR TILTED EXAM. TABLE UV-56
- K823695 — CPM METABOLIC MONITOR
- K791287 — MEDICOR QUALITY CONTROL BUFFER
- K790803 — SYRINGE TONOMETER
- K781417 — PRECISION GAS MIXER
Data sourced from openFDA. This site is unofficial and independent of the FDA.