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.

Port & Catheter, Implanted, Subcutaneous, Intraperitoneal

FDA product code LLD · 4 cleared devices

Class 2 General Hospital
Regulation
21 CFR 880.5965
Review panel
HO
Implant
Yes
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1984-03-06 – 1988-03-29
↑