Company ยท US
Neward Enterprises, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1996. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 29, 1996 | K960549 | MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE Neward Enterprises, Inc. | HDB |
| May 3, 1995 | K943938 | MITYVAC SUPER M STYLE VACUM EXTRACTOR, DISPOSABLE Neward Enterprises, Inc. | HDB |
| May 4, 1994 | K934011 | MITYVAC(R) OBSTETRIC VAC DELIV KIT W/UNIV VAC RELEASE Neward Enterprises, Inc. | HDB |
| Oct 8, 1993 | K925572 | MITYVAC DISPOS-A-PLATE DISPOSABLE LEG PLATE Neward Enterprises, Inc. | HGM |
| Jun 22, 1992 | K913324 | MITYVAC(R) SAFTISOFT OBSTETRICAL VACUUM DELIV KIT Neward Enterprises, Inc. | HDB |
| Dec 10, 1991 | K910815 | CR SPIRAL ELECTRODE Neward Enterprises, Inc. | HGP |
| Mar 31, 1989 | K890307 | MITYVAC M STYLE VACUUM EXTRACTOR, DISPOSABLE Neward Enterprises, Inc. | HDB |
| Mar 12, 1984 | K840403 | VENA * BRIDGE Neward Enterprises, Inc. |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||