Neward Enterprises, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Neward Enterprises, Inc. Obstetrics & Gynecology ✕
7 devices
Cleared
Aug 29, 1996
MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE
Obstetrics & Gynecology
203d
Cleared
May 03, 1995
MITYVAC SUPER M STYLE VACUM EXTRACTOR, DISPOSABLE
Obstetrics & Gynecology
264d
Cleared
May 04, 1994
MITYVAC(R) OBSTETRIC VAC DELIV KIT W/UNIV VAC RELEASE
Obstetrics & Gynecology
260d
Cleared
Oct 08, 1993
MITYVAC DISPOS-A-PLATE DISPOSABLE LEG PLATE
Obstetrics & Gynecology
339d
Cleared
Jun 22, 1992
MITYVAC(R) SAFTISOFT OBSTETRICAL VACUUM DELIV KIT
Obstetrics & Gynecology
333d
Cleared
Dec 10, 1991
CR SPIRAL ELECTRODE
Obstetrics & Gynecology
287d
Cleared
Mar 31, 1989
MITYVAC M STYLE VACUUM EXTRACTOR, DISPOSABLE
Obstetrics & Gynecology
67d