
KARL STORZ Endoscopy-America, Inc.
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KARL STORZ LARYNGOSCOPE ACCESSORIES is an FDA 510(k)-cleared medical device (K944295) manufactured by KARL STORZ Endoscopy-America, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 3, 1994. Regulation: 8.

ADC
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