Name: ANGIOGRAPHIC CATHETER -- MODIFICATION
Brand: Interventional Therapeutics Corp.
SKU: K922101

ANGIOGRAPHIC CATHETER -- MODIFICATION is an FDA 510(k)-cleared medical device (K922101) 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 February 11, 1993. Regulation: 8.

ANGIOGRAPHIC CATHETER -- MODIFICATION

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