
Medtronic Vascular
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MODIFIED MODELS 8320/8322/8329/8316/8317/8318 is an FDA 510(k)-cleared medical device (K861719) manufactured by Medtronic Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 30, 1986. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280