Name: PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02
Brand: Philips Medical Systems
SKU: K021422

PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02 is an FDA 510(k)-cleared medical device (K021422) manufactured by Philips Medical Systems. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 14, 2002. Regulation: 8.

PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02

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