Midmark Corp.
MODEL 561 C-ARM PROCEDURES STRETCHER
SKU K923730UPC FPO
In Stock
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IIFDA 510(k) Cleared (K923730)
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Free shipping on orders over $99 · 30-day returns
Midmark Corp.
Free shipping on orders over $99 · 30-day returns
MODEL 561 C-ARM PROCEDURES STRETCHER is an FDA 510(k)-cleared medical device (K923730) manufactured by Midmark Corp.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 8, 1994. Regulation: 8.
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