Medical Dynamics, Inc.
Medical Dynamics, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1998.
Top product codes for Medical Dynamics, Inc.
Recent clearances by Medical Dynamics, Inc.
- K974542 — TRUE VISION, TRUE VISION II
- K921294 — VIDEO ENDOSCOPE-RIGID MODIFICATION
- K934682 — SURGICAL VIDEO CAMERA AND ACCESSORIES
- K930568 — ADAIR/VERESS NEEDLE INTRODUCER SET
- K915538 — OVER THE WIRE STONE BASKET
- K914315 — OPTICAL CATHETER INTRODUCER SETS, MODIFICATION
- K913986 — CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM
- K911296 — OPTICAL CATHETER ARTHROSCOPE
- K903339 — VIDEO ENDOSCOPE, RIGID
- K904609 — XENON LIGHT SOURCE
- K904113 — OPERATIVE RECORDING CAMERA
- K900374 — ADAIR/VERESS NEEDLE INTRODUCER SET
- K896008 — MODEL 6500 MERCURY ARC LIGHT SOURCE
- K895041 — OPTICAL CATHETER(TM) INTRODUCER SETS
- K894319 — MEDICAL DYNAMICS LIGHT SOURCE
- K891983 — CAM-WRAP(TM) NEW STERILIZATION PROCEDURE
- K891236 — FDX SOLID STATE VIDEO CAMERA MODEL 5950
- K884039 — MEDICAL DYNAMICS SOLID STATE VIDEO CAMERA 5940
Data sourced from openFDA. This site is unofficial and independent of the FDA.