Origin Medsystems, Inc.
PREPERITONEAL DISTENTION BALLOON SYSTEMS (MODIFICATION)
SKU K953561UPC GCJ
In Stock
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IIFDA 510(k) Cleared (K953561)
1
Free shipping on orders over $99 · 30-day returns
Origin Medsystems, Inc.
Free shipping on orders over $99 · 30-day returns
PREPERITONEAL DISTENTION BALLOON SYSTEMS (MODIFICATION) is an FDA 510(k)-cleared medical device (K953561) manufactured by Origin Medsystems, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 10, 1995. Regulation: 8.
