Waters Assoc., Inc.
Waters Assoc., Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1981.
Top product codes for Waters Assoc., Inc.
Recent clearances by Waters Assoc., Inc.
- K811975 — MODEL 480 VARIABLE WAVELENGTH ULTRA VIOL
- K802481 — 7FRENCH FLOW DIRECTED TRIPLE LUMEN CATH
- K801852 — MRM-2 OXYGEN CONSUMPTION MONITOR
- K801431 — PAN-AM MYELOGRAM TRAY
- K791661 — SYSTEM CONTROLLER 720 SERIES
- K791026 — 4F STERILE BALLOON-LESS, CATHETER 913-28
- K782175 — CARTRIDGE HOLDER, RCM 100
- K790145 — SOLVENT DELIVERY SYSTEM
- K781805 — CARDIAC COMPUTERS, CO-10 & CO-10R
- K781915 — DATA MODULE
- K781692 — CALIBRATOR, DYNAMIC
- K781264 — PAB CONVENIENCE TRAY
- K780245 — RECORDER, RE-100P HOT STYLUS STRIP CHART
- K780031 — FLUORESCENCE DETECTOR MODEL 420
- K772311 — WISP MODEL 710
- K761166 — TC-1 CARDIAC OUTPUT COMPUTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.