
Surefire Medical, Inc.
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Surefire Spark Infusion System is an FDA 510(k)-cleared medical device (K180677) manufactured by Surefire Medical, 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 2, 2018. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280