HHWClass II
Pessary, Vaginal
21 CFR 884.3575 / Obstetrics/Gynecology
HHW is the FDA product code for Pessary, Vaginal, a class II device type, regulated under 21 CFR 884.3575. As of , FDA records hold 41 510(k) clearances under this code, the most recent dated , and 17 recalls.
Classification record
- Product code
- HHW
- Device name
- Pessary, Vaginal
- Regulation
- 21 CFR 884.3575
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 41
- Ingested recalls
- 17
Clearances, product code HHW
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1977 | 1 |
| 1978 | 1 |
| 1988 | 1 |
| 1989 | 1 |
| 1990 | 2 |
| 1992 | 1 |
| 1994 | 1 |
| 1995 | 2 |
| 1997 | 1 |
| 1998 | 3 |
| 1999 | 2 |
| 2000 | 1 |
| 2001 | 1 |
| 2002 | 2 |
| 2003 | 1 |
| 2004 | 1 |
| 2006 | 1 |
| 2008 | 1 |
| 2009 | 1 |
| 2010 | 1 |
| 2013 | 1 |
| 2014 | 2 |
| 2015 | 1 |
| 2016 | 1 |
| 2018 | 1 |
| 2019 | 2 |
| 2024 | 5 |
| 2025 | 1 |
| 2026 | 1 |
Applicants with the most clearances
Product code HHW| Applicant | Clearances |
|---|---|
| Deschutes Medical Products, Inc. | 5 |
| Panpac Medical Corporation | 4 |
| Bioteque America Inc | 3 |
| Johnson & Johnson MEDICAL GmbH | 3 |
| Contipi, Ltd. | 2 |
| CooperSurgical, Inc. | 2 |
| Eastmed, Inc. | 2 |
| Milex Products, Inc. | 2 |
| Adamed, Ltd. | 1 |
| Cntrl+, Inc. | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.