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.

Container, Liquid Medication, Graduated

FDA product code KYW · 2 cleared devices

Class 1 General Hospital
Regulation
21 CFR 880.6430
Review panel
HO
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
Yes
Clearance span
1979-08-03 – 1980-02-26
↑