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FDA 510(k), K890567, BITE BLOCK #59430
FDA 510(k), K890567, BITE BLOCK #59430
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510(K) Number: K890567
Device Name: BITE BLOCK #59430
Manufacturer: MEDI-SOURCE, INC.
Device Classification Name: block, bite
Regulation Number: 882.5070
Classification Product Code: JXL
Date Received: 02/06/1989
Decision Date: 02/17/1989
Regulation Medical Specialty: Neurology
Device Name: BITE BLOCK #59430
Manufacturer: MEDI-SOURCE, INC.
Device Classification Name: block, bite
Regulation Number: 882.5070
Classification Product Code: JXL
Date Received: 02/06/1989
Decision Date: 02/17/1989
Regulation Medical Specialty: Neurology
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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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