
Medrad, Inc.
Free shipping on orders over $99 · 30-day returns
POST EXTRA SYSTOLIC POSTENTLATOR is an FDA 510(k)-cleared medical device (K791959) manufactured by Medrad, Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 8, 1980. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280