Brilliant Ray Intl., Inc.
Brilliant Ray Intl., Inc. holds FDA 510(k) medical device clearances, cleared in 1989.
Top product codes for Brilliant Ray Intl., Inc.
Recent clearances by Brilliant Ray Intl., Inc.
- K892022 — PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY)
- K892023 — PATIENT EXAM GLOVES (MFG. XIAN WELFARE LATEX )
- K892024 — PATIENT EXAM GLOVES (MFG. CHAGAN TANG CAPITOL)
- K892025 — PATIENT EXAM GLOVES (MFG. BEIJING LATEX FACTORY)
- K892109 — PATIENT EXAMINATION GLOVES (LATEX)
- K891739 — PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY
- K891740 — PATIENT EXAM GLOVES (LATEX) MFG. TIANJIN KANG BAO
Data sourced from openFDA. This site is unofficial and independent of the FDA.