Product code HDG— Obstetrics/Gynecology
SPECULUM, VAGINAL, METAL FIBEROPTIC
- Classification name
- Speculum, Vaginal, Metal, Fiberoptic
- Device class
- Class 1
- Regulation
- 21 CFR 884.4520
- Advisory panel
- Obstetrics/Gynecology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code HDG
FDA has cleared devices under product code HDG between 1977 and 1987, filed by 2 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1987
- 1977
Top applicants under product code HDG
Recent clearances under product code HDG
Data sourced from openFDA. This site is unofficial and independent of the FDA.