
Pace Tech Medical Monitors, Inc.
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VITALMAX 4000 CONFIGURED/VITALMAX 4000 MODULAR/VITALMAX 4100/MINIPACK 3100/3000/VITALMAX 800+/MINIPACK 300 is an FDA 510(k)-cleared medical device (K970445) manufactured by Pace Tech Medical Monitors, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 29, 1998. Regulation: 8.

ADC
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