Lien Chang Rubber Industrial Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K891938 | NON-STERILE PATIENT EXAMINATION GLOVES | LYY | 1989-05-08 | View |
| 510(k) | K881664 | LATEX SURGICAL GLOVE | KGO | 1989-01-06 | View |
No matching devices.
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