Name: OCCLUSION BALLON CATHETER MODIFICAION
Brand: Interventional Therapeutics Corp.
SKU: K921399

OCCLUSION BALLON CATHETER MODIFICAION is an FDA 510(k)-cleared medical device (K921399) manufactured by Interventional Therapeutics 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 September 24, 1992. Regulation: 8.

OCCLUSION BALLON CATHETER MODIFICAION

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