Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Screw, Fibroid, Gynecological

FDA product code HHO · 2 cleared devices

Class 2 Obstetrics/Gynecology
Regulation
21 CFR 884.4530
Review panel
OB
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1992-05-18 – 1992-05-18
↑