Endoscopic Technologies, Inc.
Endoscopic Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2006.
Top product codes for Endoscopic Technologies, Inc.
Recent clearances by Endoscopic Technologies, Inc.
- K060101 — ESTECH AORTIC EASY FLOW CANNULA
- K053326 — ESTECH COBRA ELECTROSURGICAL UNIT & CABLE
- K053100 — ESTECH COBRA BIPOLAR SYSTEM
- K946105 — ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES
- K945978 — TUBING, NONINVASIVE
- K945979 — TROCAR/CANNULA
- K924057 — DISPOSIBLE ELECTRO COAGULATION PROBE
- K922685 — TROCARS
Data sourced from openFDA. This site is unofficial and independent of the FDA.