Meadox Surgimed, Inc.
Meadox Surgimed, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1995.
Top product codes for Meadox Surgimed, Inc.
Recent clearances by Meadox Surgimed, Inc.
- K944143 — MS CLASSIQUE BALLOON CATHETER
- K945061 — NOPROFILE OLBERT CATHETER SYSTEM
- K942382 — MS AMPLATZ EXTRA STIFF GUIDE WIRE
- K930201 — ACECUT SUTOMATIC BIOPSY SYSTEM
- K911635 — MEADOX(R) SURGIMED(R) BIOPSY GUN II
- K905181 — NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGY
- K904582 — QUICKWIRE - HYDROPHILIC COATED GUIDEWIRE
- K904983 — MEADOX(R) SURGIMED OLBERT CATH SYST FOR UROLOGY
- K902461 — MEADOX SURGIMED BIOPSY GUN AND NEEDLE
- K890926 — SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLE
- K863218 — CYTOSTATIC FILTRATION SET
- K861267 — UROCUT BIOPSY NEEDLE
- K862742 — NEPHROSTOMY SET
- K862550 — OLBERT CATHETER SYSTEM WITH SIDEWINDER CURVE
- K860430 — THE NAVIGATOR STEERABLE GUIDE WIRE
- K861220 — LUNDERQUIST - RING PTC DRAINAGE CATHETER
- K860429 — MEADOX SURGIMED GUIDE CATHETER
- K854262 — MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY
- K854404 — ROTEX SCREW BIOPSY NEEDLE
- K854420 — MEADOX SURGIMED A/S THREE PIECE SCREW BIOPSY NEEDL
- K851647 — OLBERT CATHETER SYSTEM FOR BILIARY TRACT DILATATIO
- K851463 — OLBERT CATHETER SYS FOR URETERAL DILATION
- K843798 — MEADOX SURGIMED A/S CATHETER SHEATH SYS
- K841704 — THINWALL PUNCTURE NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.