Ampri Rubberware Industries Sdn Bhd
Ampri Rubberware Industries Sdn Bhd holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1999.
Top product codes for Ampri Rubberware Industries Sdn Bhd
Recent clearances by Ampri Rubberware Industries Sdn Bhd
- K990677 — ABSOGEL CHEMOTHERAPHY GLOVES
- K990812 — POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTA
- K954002 — AMPRI
- K952833 — AMPRI
- K945948 — ABSOGEL STERILE POWDER-FREE SURGICAL GLOVES
- K946056 — ABSOGEL NON-STERILE EXAMINATION GLOVES (POWDER-FREE)
- K892176 — CORRECT TOUCH SURGEONS GLOVES
- K892175 — CORRECT TOUCH EXAMINATION GLOVES (LATEX)
Data sourced from openFDA. This site is unofficial and independent of the FDA.