Ampri Rubberware Industries Sdn Bhd
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K990677 | ABSOGEL CHEMOTHERAPHY GLOVES | LZC | 1999-11-01 | View |
| 510(k) | K990812 | POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTA | LYY | 1999-05-04 | View |
| 510(k) | K954002 | AMPRI | KGO | 1996-01-29 | View |
| 510(k) | K952833 | AMPRI | LYY | 1995-09-05 | View |
| 510(k) | K945948 | ABSOGEL STERILE POWDER-FREE SURGICAL GLOVES | KGO | 1995-07-31 | View |
| 510(k) | K946056 | ABSOGEL NON-STERILE EXAMINATION GLOVES (POWDER-FREE) | LYY | 1995-07-20 | View |
| 510(k) | K892176 | CORRECT TOUCH SURGEONS GLOVES | KGO | 1989-09-06 | View |
| 510(k) | K892175 | CORRECT TOUCH EXAMINATION GLOVES (LATEX) | LYY | 1989-08-25 | View |
No matching devices.
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