HGD — Applicator, Vaginal Class I
FDA product code HGD covers "Applicator, Vaginal", a Class I medical device regulated under 21 CFR 884.4520. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- HGD
- Device Class
- Class I
- Regulation Number
- 884.4520
- Submission Type
- Review Panel
- OB
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K823517 | kline technologies | THE KLINE APPLICATOR | January 18, 1983 |