Optovent AB
1 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| OPTOVENT RESPONS, OPTOVENT RENEE (OPTOVENT RESPONS WITHOUT PULSE OXIMETRY MODULE) (K003704) | Optovent AB | 2001-02-05 |
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Every clearance here is in the API, with alerts when new ones post.