HFF — Aspirator, Endometrial Class II
FDA product code HFF covers "Aspirator, Endometrial", a Class II medical device regulated under 21 CFR 884.1060. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 5 recent 510(k) clearances have been granted under this product code.
Classification details
- Product Code
- HFF
- Device Class
- Class II
- Regulation Number
- 884.1060
- Submission Type
- 510(k)
- Review Panel
- OB
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No
Recent 510(k) clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K041237 | Gynetics Medical Products | ECHOSAMPLER | Sep 8, 2004 |
| K903002 | Gynopharma | PROBET (TM) | Apr 5, 1991 |
| K902693 | Wallach Surgical Devices | WALLACH FLEXIBLE ENDOMETRIAL SAMPLER | Jan 31, 1991 |
| K831212 | Axcan Scientific | ENDOSCANN | Jun 15, 1984 |
| K820641 | Axcan Scientific | ACCURETTE | Jun 22, 1982 |