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FDA 510(k), K780181, GLOVES, FLOOR
FDA 510(k), K780181, GLOVES, FLOOR
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510(K) Number: K780181
Device Name: GLOVES, FLOOR
Manufacturer:
Device Classification Name: Chair, Blood Donor
Regulation Number: FML
Classification Product Code: 02/03/1978
Date Received: 02/21/1978
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: GLOVES, FLOOR
Manufacturer:
Device Classification Name: Chair, Blood Donor
Regulation Number: FML
Classification Product Code: 02/03/1978
Date Received: 02/21/1978
Decision Date: Substantially Equivalent (SESE)
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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