The Procter & Gamble Co.
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) | K110669 | TAMPAX C PLASTIC TAMPONS, UNSCENTED | HEB | 2011-06-02 | View |
| 510(k) | K091419 | VICKS POWERSHOT DRY THROAT & MOUTH RELIEF | LFD | 2009-08-28 | View |
No matching devices.
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