Neward Enterprises, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K960549 | MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE | August 29, 1996 |
| K943938 | MITYVAC SUPER M STYLE VACUM EXTRACTOR, DISPOSABLE | May 3, 1995 |
| K934011 | MITYVAC(R) OBSTETRIC VAC DELIV KIT W/UNIV VAC RELEASE | May 4, 1994 |
| K925572 | MITYVAC DISPOS-A-PLATE DISPOSABLE LEG PLATE | October 8, 1993 |
| K913324 | MITYVAC(R) SAFTISOFT OBSTETRICAL VACUUM DELIV KIT | June 22, 1992 |
| K910815 | CR SPIRAL ELECTRODE | December 10, 1991 |
| K890307 | MITYVAC M STYLE VACUUM EXTRACTOR, DISPOSABLE | March 31, 1989 |
| K840403 | VENA * BRIDGE | March 12, 1984 |