FDA 510(k) Applications Submitted by OPTOVENT AB
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K003704 | 12/01/2000 | OPTOVENT RESPONS, OPTOVENT RENEE (OPTOVENT RESPONS WITHOUT PULSE OXIMETRY MODULE) | OPTOVENT AB |
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