Ametek, Inc.
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) | K943824 | GASEOUS OXYGEN ANALYZER (MODEL S-3A) MODIFICATION | CCL | 1996-11-01 | View |
| 510(k) | K942113 | CARBON DIOXIDE ANALYZER (MODEL CD-3A) | CCK | 1995-02-16 | View |
No matching devices.
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