
Agilent Technologies, Inc.
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AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154 is an FDA 510(k)-cleared medical device (K011093) manufactured by Agilent Technologies, 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 April 30, 2001. Regulation: 8.

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280

Medline
SKU MSC192133

Medline
SKU DX887514