
Parexel Intl. Corp.
Free shipping on orders over $99 · 30-day returns
ACTA METRA/ACTA GNOSIS FIRMWARE PACKAGE is an FDA 510(k)-cleared medical device (K900385) manufactured by Parexel Intl. Corp.. 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 8, 1991. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280