
Camino Laboratories, Inc.
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MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM is an FDA 510(k)-cleared medical device (K893232) manufactured by Camino Laboratories, 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 July 13, 1989. Regulation: 8.

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