LATEX PATIENT EXAMINATION GLOVE— 510(k) K894796
Substantially EquivalentBh Limela Industries Sdn. Bhd.
FDA 510(k) clearance K894796 for LATEX PATIENT EXAMINATION GLOVE, Substantially Equivalent on 1989-09-26. Applicant: Bh Limela Industries Sdn. Bhd.. Device class: 1.
Clearance details
- Applicant
- Bh Limela Industries Sdn. Bhd.
- Product code
- Code LYY
- Device class
- Class 1
- Regulation
- 21 CFR 880.6250
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Estate, 13600 Prai, P.W., MY
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Data sourced from openFDA. This site is unofficial and independent of the FDA.