Arvey Corp.
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) | K843182 | MASTER-CHEK BOWIE-DICK TYPE TEST | JOJ | 1984-10-09 | View |
| 510(k) | K821997 | MEDI + BIO SAFE STEAM STERILIZ. INDICAT | JOJ | 1982-08-16 | View |
No matching devices.
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