PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE)— 510(k) K962650
Substantially EquivalentSti Medical Sdn Bhd
FDA 510(k) clearance K962650 for PATIENT LATEX EXAMINATION GLOVES (POWDERED, NON STERILE), Substantially Equivalent on 1996-08-15. Applicant: Sti Medical Sdn Bhd. Device class: 1.
Clearance details
- Applicant
- Sti Medical 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
- Selangor, MY
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More clearances from Sti Medical Sdn Bhd
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