KARL STORZ Endoscopy-America, Inc.
KARL STORZ GELET URETERO-RENOSCOPES/KARL STORZ ALKEN MOTION CONTROL DEVICE
SKU K960323UPC FGB
In Stock
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IIFDA 510(k) Cleared (K960323)
1
Free shipping on orders over $99 · 30-day returns
KARL STORZ Endoscopy-America, Inc.
Free shipping on orders over $99 · 30-day returns
KARL STORZ GELET URETERO-RENOSCOPES/KARL STORZ ALKEN MOTION CONTROL DEVICE is an FDA 510(k)-cleared medical device (K960323) manufactured by KARL STORZ Endoscopy-America, 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 April 21, 1996. Regulation: 8.
