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FDA 510(k), K200500, Molekule Air Pro RX
FDA 510(k), K200500, Molekule Air Pro RX
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$149.00 USD
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$149.00 USD
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510(K) Number: K200500
Device Name: Molekule Air Pro RX
Manufacturer: Molekule, Inc.
Device Classification Name: Purifier, Air, Ultraviolet, Medical
Regulation Number: 880.6500
Classification Product Code: FRA
Date Received: 02/28/2020
Decision Date: 04/15/2020
Regulation Medical Specialty: General Hospital
Device Name: Molekule Air Pro RX
Manufacturer: Molekule, Inc.
Device Classification Name: Purifier, Air, Ultraviolet, Medical
Regulation Number: 880.6500
Classification Product Code: FRA
Date Received: 02/28/2020
Decision Date: 04/15/2020
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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