KSEA ENDOSCOPES FOR DENTAL PROCEDURES

KSEA ENDOSCOPES FOR DENTAL PROCEDURES is an FDA 510(k)-cleared medical device (K982658) manufactured by KARL STORZ Endoscopy-America, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 14, 1998. Regulation: 8.