Beacon Laboratories, Inc.
Beacon Laboratories, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1994.
Top product codes for Beacon Laboratories, Inc.
Recent clearances by Beacon Laboratories, Inc.
- K930243 — FLEXIBLE EXTENDER
- K930497 — ARGON HANDPIECES
- K925708 — DISPOSABLE ELECTROSURGERY BALL ELECTRODE
- K922289 — SESQUIPOLAR(TM) MIS ELECTRODE
- K925619 — DISPOSABLE HAND-SWITCHING ESU PENCIL
- K915788 — MIS ELECTROSURGICAL ELECTRODES
- K920100 — GSU HANDPIECE ADAPTER
- K913772 — PRESSURE GUARD
- K905752 — ARGON BEAM COMBO LAPAROSCOPIC ELECTRODE
- K904506 — ACTIVE ADAPTER
- K902996 — ARGON BEAM LAPAROSCOPIC ELECTRODE
- K903724 — BEAMER 1,2,4,6, AND 8
- K902035 — FLEXIBLE EXTENDER
- K900767 — B-300 COMBINATION SWITCHING DISPOSABLE HANDPIECE
- K901248 — ABC HANDPIECE ADAPTER
- K894663 — BEAMER ONE
- K894762 — B100 DISPOSABLE HANDPIECE
- K894602 — B1 FOOTSWITCH (SINGLE PEDDLE), B2 (DOUBLE PEDDLE)
Data sourced from openFDA. This site is unofficial and independent of the FDA.