Neward Enterprises, Inc.
Neward Enterprises, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1996.
Top product codes for Neward Enterprises, Inc.
Recent clearances by Neward Enterprises, Inc.
- K960549 — MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE
- K943938 — MITYVAC SUPER M STYLE VACUM EXTRACTOR, DISPOSABLE
- K934011 — MITYVAC(R) OBSTETRIC VAC DELIV KIT W/UNIV VAC RELEASE
- K925572 — MITYVAC DISPOS-A-PLATE DISPOSABLE LEG PLATE
- K913324 — MITYVAC(R) SAFTISOFT OBSTETRICAL VACUUM DELIV KIT
- K910815 — CR SPIRAL ELECTRODE
- K890307 — MITYVAC M STYLE VACUUM EXTRACTOR, DISPOSABLE
- K840403 — VENA * BRIDGE
Data sourced from openFDA. This site is unofficial and independent of the FDA.