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FDA 510(k), K820454, THE RED CAP
FDA 510(k), K820454, THE RED CAP
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$89.00 USD
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510(K) Number: K820454
Device Name: THE RED CAP
Manufacturer: BURRON MEDICAL PRODUCTS, INC.
Device Classification Name: syringe, piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 02/18/1982
Decision Date: 03/08/1982
Regulation Medical Specialty: General Hospital
Device Name: THE RED CAP
Manufacturer: BURRON MEDICAL PRODUCTS, INC.
Device Classification Name: syringe, piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 02/18/1982
Decision Date: 03/08/1982
Regulation Medical Specialty: General Hospital
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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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