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FDA 510(k), K893334, PREPOWDERED VINYL EXAM GLOVES
FDA 510(k), K893334, PREPOWDERED VINYL EXAM GLOVES
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510(K) Number: K893334
Device Name: PREPOWDERED VINYL EXAM GLOVES
Manufacturer: DYNAREX CORP.
Device Classification Name: vinyl patient examination glove
Regulation Number: 880.6250
Classification Product Code: LYZ
Date Received: 04/20/1989
Decision Date: 08/15/1989
Regulation Medical Specialty: General Hospital
Device Name: PREPOWDERED VINYL EXAM GLOVES
Manufacturer: DYNAREX CORP.
Device Classification Name: vinyl patient examination glove
Regulation Number: 880.6250
Classification Product Code: LYZ
Date Received: 04/20/1989
Decision Date: 08/15/1989
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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