# Ampri Rubberware Industries Sdn Bhd

- Location (FDA's records): Selangor, MY
- FDA decisions: 8 (1989–1999): 8 510(k) clearances
- Product codes: LYY (4), KGO (3), LZC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K990677: Absogel Chemotheraphy Gloves (Nov 1, 1999)
- K990812: Powder-Free Latex Examination Glove with Protein Labeling Claim (Contains 50 Micrograms or Less  of Total Water Extracta (May 4, 1999)
- K954002: AMPRI (Jan 29, 1996)
- K952833: AMPRI (Sep 5, 1995)
- K945948: Absogel Sterile Powder-Free Surgical Gloves (Jul 31, 1995)
- K946056: Absogel Non-Sterile Examination Gloves (Powder-Free) (Jul 20, 1995)
- K892176: Correct Touch Surgeons Gloves (Sep 6, 1989)
- K892175: Correct Touch Examination Gloves (Latex) (Aug 25, 1989)

Source page: https://510kreport.com/company/ampri-rubberware-industries-sdn-bhd