Aladan Corp.
FDA 510(k) & PMA Approved Devices — 18 products
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Total Devices18
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K960590 | TRI-CLEAN 110/TRI-CLEAN PLUS GLOVE | LYY | 1996-10-31 | View |
| 510(k) | K952404 | SAFETEX SUPER HYPERALLERGENIC POWDERFREE LATEX MEDICAL GLOVE | LYY | 1995-07-20 | View |
| 510(k) | K952556 | SAFETEX SUPER HYPOALLERGENIC POWDERED LATEX EXAMINATION GLOVE | LYY | 1995-06-26 | View |
| 510(k) | K943933 | SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM | HIS | 1995-06-22 | View |
| 510(k) | K951839 | ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES | LYY | 1995-06-15 | View |
| 510(k) | K943883 | SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM | HIS | 1995-04-14 | View |
| 510(k) | K942758 | HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE | LYY | 1994-07-08 | View |
| 510(k) | K940873 | SAFETEX HYPOALLERGENIC POWDERFREE LATEX EXAMINATION GLOVE | LYY | 1994-04-22 | View |
| 510(k) | K911774 | ALADAN LATEX MEDICAL GLOVE | LYY | 1991-05-03 | View |
| 510(k) | K911447 | LATEX EXAMINATION GLOVES (HYPOALLERGENIC) | LYY | 1991-04-16 | View |
| 510(k) | K905279 | CONDOM (RUBBER) CONTRACEPTIVE | HIS | 1991-02-19 | View |
| 510(k) | K905678 | ALADERM | LYY | 1991-01-18 | View |
| 510(k) | K902565 | ALADAN TRI-CLEAN 110 POWDERLESS LATEX GLOVE | LYY | 1990-07-03 | View |
| 510(k) | K901416 | CONDOM (RUBBER) CONTRACEPTIVE | HIS | 1990-06-04 | View |
| 510(k) | K902181 | MODIFIED NON-STERILE LATEX EXAMINATION GLOVES | LYY | 1990-06-01 | View |
| 510(k) | K902182 | MODIFIED STERILE LATEX EXAMINATION GLOVES | LYY | 1990-06-01 | View |
| 510(k) | K890880 | ALADAN STERILE LATEX MEDICAL GLOVE | LYY | 1989-03-29 | View |
| 510(k) | K890627 | UNSTERILE PATIENT EXAMINATION GLOVE | LYY | 1989-03-23 | View |
No matching devices.
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