KSEA DE LA PLAZA BLEPHAROPLASTY SET

KSEA DE LA PLAZA BLEPHAROPLASTY SET is an FDA 510(k)-cleared medical device (K991592) manufactured by KARL STORZ Endoscopy-America, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 1, 1999. Regulation: 8.