Biodan Medical Systems, Ltd.
Biodan Medical Systems, Ltd. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1993.
Top product codes for Biodan Medical Systems, Ltd.
Recent clearances by Biodan Medical Systems, Ltd.
- K932153 — THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROME
- K930261 — RTM REHABILITATION TREADMILL, MODEL #945-200
- K930262 — TREATMENT TABLE, MODEL #825-100
- K930259 — TRACTION TABLE MODEL #825-200
- K926083 — NUCLEAR PATIENT SANNING TABLES, VARIOUS TYPES
- K926082 — CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT
- K922591 — UROLOGICAL C-ARM TABLE, MODEL #056-450
- K922604 — DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE
- K922605 — TRENDELENBURG ULTRASOUND TABLE, MODEL # 056-603
- K923350 — CLOSED CHAIN ATTACHMENT, MODEL #820-520
- K922772 — TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR
- K922602 — CABLE COLUMN WEIGHT SYSTEM MODEL #940-200
- K922603 — TOTAL WORK INTEGRATOR, MODEL #940-110
- K922606 — MULTI JOINT WEIGHT SYSTEM MODEL #940-100
- K922092 — SINGLE CHAIR INTEGRAL BACK ATTACHMENT
- K921501 — DELUXE C ARM RADIOLOGICAL TABLE, MODEL #056-004
- K900770 — HOME URODATA SYSTEM(TM)
- K840088 — BIODEX ACT-O-KIT TSH-RIA-
- K832896 — LEGIONELLA INDIRECT FLUORESCENT ANTIBOD
- K822066 — LEGIONELLA PNEUMOPHILA
Data sourced from openFDA. This site is unofficial and independent of the FDA.