Promex, Inc.
Promex, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2002.
Top product codes for Promex, Inc.
Recent clearances by Promex, Inc.
- K023450 — BIOPSY SITE TISSUE MARKER DEVICE
- K022634 — CO-AXIAL INTRODUCER NEEDLE
- K010400 — VACUUM ASSISTED CORE BIOPSY DEVICE
- K011270 — AUTOMATED CORE BIOPSY DEVICE
- K001132 — BONE BIOPSY NEEDLE
- K994272 — AUTOMATED CORE BIOPSY DEVICE
- K993435 — MANUAL BONE MARROW BIOPSY DEVICE
- K973184 — PROSTATE SEEDING NEEDLE
- K972865 — PROMEX ENT TISSUE REMOVAL SYSTEM
- K961078 — AUTOMATED VITRECTOMY DEVICE
- K960023 — KIRSHNER WIRES (K-WIRE) & STEINMANN PINS
- K960405 — SPINAL NEEDLE
- K955168 — SURGICAL CUTTER
- K954265 — TROCAR STYLE NEEDLE/CO-AXIAL INTRODUCER NEEDLE
- K954231 — AUGASTROENTEROLOGY-UROLOGY BIOPSY INSTRUMENT
- K954155 — GREENE, TURNER, MENGHINI STYLE ASPIRATION BIOPSY NEEDLE
- K945146 — CHIBA, FRANSEEN, WESTCOTT, SPINAL STYLE ASPIRATION BIOPSY NEEDLE
- K945124 — BREAST LESION LOCALIZATION NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.