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FDA 510(k), K913207, TRIFLEX(R) POWDER FREE STERILE SURGEON'S GLOVE
FDA 510(k), K913207, TRIFLEX(R) POWDER FREE STERILE SURGEON'S GLOVE
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510(K) Number: K913207
Device Name: TRIFLEX(R) POWDER FREE STERILE SURGEON'S GLOVE
Manufacturer: STEPHEN A CAMPBELL
Device Classification Name: Surgeon'S Gloves
Regulation Number: KGO
Classification Product Code: 07/19/1991
Date Received: 09/11/1991
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: TRIFLEX(R) POWDER FREE STERILE SURGEON'S GLOVE
Manufacturer: STEPHEN A CAMPBELL
Device Classification Name: Surgeon'S Gloves
Regulation Number: KGO
Classification Product Code: 07/19/1991
Date Received: 09/11/1991
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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