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.

Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia

FDA product code KLK · 47 cleared devices

Class 2 Anesthesiology
Regulation
21 CFR 868.2500
Review panel
AN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1978-10-10 – 2001-05-04
↑