HGF — Source, Abortion Unit, Vacuum Class II
FDA product code HGF covers "Source, Abortion Unit, Vacuum", a Class II medical device regulated under 21 CFR 884.5070. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 4 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- HGF
- Device Class
- Class II
- Regulation Number
- 884.5070
- Submission Type
- Review Panel
- OB
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K945179 | medgyn products | BOTTLE COLLECTION SET | January 26, 1995 |
| K905115 | douglas james donaldson compliance services | BIOVISION ENDOCULAR PROBE | February 11, 1991 |
| K904248 | charles l. rose and co | MODEL GLASE 210 HOLMIUM LASER SYSTEM | December 14, 1990 |
| K890787 | hgm medical laser systems | O-020 LASER INDIRECT OPHTHALMOSCOPE | March 24, 1989 |