Bovie Medical
Bovie Medical holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2010.
Top product codes for Bovie Medical
Recent clearances by Bovie Medical
- K092149 — BOSS COAGULATION DEVICE, MODEL BOSS1215, BOSS COAGULATION DEVICE, ANGLED ACCESS, MODEL BOSA1215
- K091440 — LAPAROSCOPIC RESECTION DEVICE, MODEL SR326L
- K090586 — BOVIE ICON GS ELECTROSURGICAL GENERATOR (GS100), HANDPIECE (GS-OP-R), REUSABLE HANDPIECE CABLE (GS807-RC)
- K082568 — SALINE ENHANCED ELECTROSURGICAL RESECTION (SEER) DEVICE
- K082109 — BOVIE ICON GENERAL PURPOSE RF GENERATOR
- K081431 — MEG LAPAROSCOPIC ELECTRODES
- K072041 — BOVIE IDS-400 ELECTROSURGICAL GENERATOR
- K061884 — BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120
Data sourced from openFDA. This site is unofficial and independent of the FDA.