B. Braun of America, Inc.
B. Braun of America, Inc. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2000.
Top product codes for B. Braun of America, Inc.
Recent clearances by B. Braun of America, Inc.
- K993024 — CELSITE IMPLANTABLE PORT WITH VALVED CATHETER
- K983794 — CHEMO MINI SPIKE PLUS
- K946170 — COMFORT-Q SUBCUTANEOUS INJECTION SETS
- K945850 — BRAUN DIACAN(R) FISTULA NEEDLES
- K942988 — FILTERED EXTENSION SETS
- K945752 — CELSITE(TM) BRACHIAL VENOUS PORT
- K945551 — CELSITE(TM) DUAL VENOUS SYSTEM
- K943770 — LOW VOLUME MULTIPORT
- K950982 — B. BRAUN SONOCAN BIOPSY NEEDLE AND ASPIRATION HANDLE
- K950184 — B. BRAUN IV START KITS
- K943181 — DISPENSING PIN WITH ONE-WAY VALVE
- K940980 — CHARGED SUPOR(R) FILTER EXTENSION SET
- K932569 — PENCIL POINT SPINAL NEEDLE AND TRAY
- K932400 — ESPOCAN COMBINED SPINAL/EPIDURAL NEEDLE SET & TRAY
- K925285 — DUALTHERM(R) CARDIAC OUTPUT COMPUTER
- K925401 — IV FLUID TRANSFER PIN
- K915421 — GUIDEWIRE INTRODUCER SET
- K910503 — DISCOGRAPHY KIT
- K911415 — TRUMPET VALVE
Data sourced from openFDA. This site is unofficial and independent of the FDA.