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FDA 510(k), K203434, BlueStar Rx
FDA 510(k), K203434, BlueStar Rx
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510(K) Number: K203434
Device Name: BlueStar Rx
Manufacturer: WellDoc, Inc
Device Classification Name: Calculator, Drug Dose
Regulation Number: 868.1890
Classification Product Code: NDC
Date Received: 11/23/2020
Decision Date: 09/08/2021
Regulation Medical Specialty: Anesthesiology
Device Name: BlueStar Rx
Manufacturer: WellDoc, Inc
Device Classification Name: Calculator, Drug Dose
Regulation Number: 868.1890
Classification Product Code: NDC
Date Received: 11/23/2020
Decision Date: 09/08/2021
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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